Titus Hendrik Jan Huisman

Titus Hendrik Jan Huisman's AcademicInfluence.com Rankings

Biology

#3022

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#4682

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Biochemistry

#254

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#318

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Biology

Titus Hendrik Jan Huisman's Degrees

PhD Biochemistry University of Amsterdam

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Titus Hendrik Jan Huisman's Published Works

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Published Works

Studies on the heterogeneity of hemoglobin. IX. The use of Tris(hydroxymethyl)aminomethanehcl buffers in the anion-exchange chromatography of hemoglobins. (1965) (513)
DNA sequence variation associated with elevated fetal G gamma globin production. (1985) (373)
The hemoglobinopathies: Techniques of identification (1977) (306)
Separation of tryptic peptides of normal and abnormal a, β, γ, and δ hemoglobin chains by high-performance liquid chromatography (1979) (279)
Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin. (1968) (267)
Separation of human hemoglobins by DEAE-cellulose chromatography using glycine-KCN-NaC1 developers. (1976) (248)
Determination of the Glycosylated Hemoglobins (Hb AI) with a New Microcolumn Procedure: Suitability of the Technique for Assessing the Clinical Management of Diabetes Mellitus (1978) (230)
Studies on the heterogeneity of hemoglobin. 13. Chromatography of various human and animal hemoglobin types on DEAE-Sephadex. (1968) (216)
Microchromatography of hemoglobins. II. A simplified procedure for the determination of hemoglobin A2. (1975) (191)
Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography. (1986) (178)
Studies on the heterogeneity of hemoglobin. I. The heterogeneity of different human hemoglobin types in carboxymethylcellulose and in amberlite IRC-50 chromatography qualitative aspects. (1960) (169)
A new high-performance liquid chromatographic procedure for the separation and quantitation of various hemoglobin variants in adults and newborn babies. (1983) (159)
Studies on the heterogeneity of hemoglobin. V. Binding of hemoglobin with oxidized glutathione. (1962) (148)
Chromatography of hemoglobin types on carboxymethylcellulose. (1958) (147)
Hemoglobin Richmond, a human hemoglobin which forms asymmetric hybrids with other hemoglobins. (1969) (133)
Microchromatography of hemoglobins. II. A rapid method for the determination of hemoglobin A2. (1974) (123)
Molecular analysis of the high-hemoglobin-F phenotype in Saudi Arabian sickle cell anemia. (1987) (118)
Fetal erythropoiesis following bone marrow transplantation. (1976) (114)
Hemoglobin Kenya, the product of fusion of amd polypeptide chains. (1972) (114)
Changes in the haemoglobin types of sheep as a response to anaemia. (1964) (105)
Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes. (1992) (104)
The Chromatography of Hemoglobin (1980) (96)
Molecular Characterization of α-Thalassemia Determinants, β-Thalassemia Alleles, and βs Haplotypes among Kuwaiti Arabs (1994) (94)
Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes (1991) (93)
NORMAL AND ABNORMAL HUMAN HEMOGLOBINS. (1963) (93)
Haplotypes of beta S chromosomes among patients with sickle cell anemia from Georgia. (1986) (87)
Studies on the heterogeneity of hemoglobin. XIV. Chromatography of normal and abnormal human hemoglobin types on CM-Sephadex. (1969) (84)
Separation of hemoglobins and hemoglobin chains by high-performance liquid chromatography. (1987) (84)
Gamma thalassemia resulting from the deletion of a gamma-globin gene (1983) (82)
Chromatographic estimation of four different human hemoglobins. (1955) (81)
The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes (1984) (80)
Hemoglobin C in Newborn Sheep and Goats: A Possible Explanation for its Function and Biosynthesis (1969) (79)
β-Thalassemia in Turkey (1990) (78)
Studies on the heterogeneity of hemoglobin : IV. Chromatographic behavior of different human hemoglobins on anion-exchange cellulose (DEAE-cellulose) (1962) (72)
Postnatal Changes in the Chemical Heterogeneity of Human Fetal Hemoglobin (1971) (72)
Hemoglobin Freiburg: Abnormal Hemoglobin Due to Deletion of a Single Amino Acid Residue (1966) (70)
Differences in Affinity of Variant β Chains for a Chains: A Possible Explanation for the Variation in the Percentages of β Chain Variants in Heterozygotes (1977) (70)
Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1‐globin variant, observed in combination with the ‐(α)20.5 KB α‐thal‐1 deletion in two Turkish patients (1993) (69)
The detection of β-globin gene mutations in β-thalassemia using oligonucleotide probes and amplified DNA (1988) (69)
Hb H disease in a Turkish family resulting from the interaction of a deletional α‐thalassaemia‐1 and a newly discovered poly A mutation (1992) (68)
Inhomogeneity of hemoglobin. VI. The minor hemoglobin components of cord blood. (1962) (68)
The structure of goat hemoglobins. I. Structural studies of the beta chains of the hemoglobins of normal and anemic goats. (1967) (66)
An Initiation Codon Mutation as a Cause of a β-Thalassemia (1990) (66)
Quantitation of hemoglobin components by high‐performance cation‐exchange liquid chromatography: Its use in diagnosis and in the assessment of cellular distribution of hemoglobin variants (1984) (66)
Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant. (1990) (64)
An improved method for quantitative determination of human fetal hemoglobin. (1970) (63)
Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent beta-thalassemia. (1970) (62)
Access to a syllabus of human hemoglobin variants (1996) via the World Wide Web. (1998) (62)
Trimodality in Tie Percentages of β Chain Variants in Heterozy-Gotes: The Effect of the Number of Aczive HBα Structural Loci (1977) (61)
Quantitation of three types of gamma chain of HbF by high pressure liquid chromatography; application of this method to the HbF of patients with sickle cell anemia or the S-HPFH condition. (1981) (60)
Sheep Hæmoglobins: Some Genetic and Physiological Aspects of Two Different Adult Hæmoglobins in Sheep (1958) (60)
World-wide occurrence of nonallelic genes for the -chain of human foetal haemoglobin in newborns. (1972) (60)
Further Nodification of the Mtcrochromatographic Deternination of Hemoglobin A (1977) (59)
Minor hemoglobins in sickle cell anemia, beta-thalassemia, and related conditions: a study of red cell fractions isolated by density gradient centrifugation. (1975) (58)
Hemoglobin Kenya, the product of a gamma-beta fusion gene: studies of the family. (1973) (58)
The structure of goat hemoglobins. II. Structural studies of the alpha chains of the hemoglobins A and B. (1968) (58)
On the chromatographic heterogeneity of human fetal hemoglobin. (1979) (57)
The detection and estimation of fetal hemoglobin by means of the alkali denaturation test. (1956) (56)
The thalassemia repository (Ninth Edition; Part II). (1998) (56)
Investigations on the amino acid composition of a macroglobulin and a cryoglobulin. (1955) (55)
Studies on an abnormal minor hemoglobin component (Hb-B2). (1961) (54)
A new high-performance liquid chromatographic procedure to quantitate hemoglobin A1c and other minor hemoglobins in blood of normal, diabetic, and alcoholic individuals. (1983) (53)
Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians. (1991) (53)
Studies on the heterogeneity of hemoglobin (1960) (52)
Hereditary persistence of fetal hemoglobin. Heterogeneity of fetal hemoglobin in homozygotes and in conjunction with -thalassemia. (1971) (51)
Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114. (1988) (51)
Partial deletion of the 5' beta-globin gene region causes beta zero-thalassemia in members of an American black family. (1984) (50)
On the levels of hemoglobins F and A2 in sickle-cell anemia and some related disorders. (1974) (50)
The amino acid sequence of the δ-β chains of hemoglobin LeporeAugusta = LeporeWashington (1966) (49)
The structure of sheep hemoglobins: II. The amino acid composition of the tryptic peptides of the non-α chains of hemoglobins A, B, C, and F (1966) (49)
Red Cell 2,3-Diphosphoglycerate and Oxygen Affinity in Newborn Goats and Sheep (1971) (49)
Two novel arrangements of the human fetal globin genes: Gγ-Gγ and Aγ-Aγ (1984) (48)
Quantitation of hemoglobin alpha chains in adult and fetal goats; gene duplication and the production of polypeptide chains. (1969) (47)
A Search for Anomalies in the ζ,α,β, and γ Globin Gene Arrangements in Normal Black, Italian, Turkish, and Spanish Newborns (1989) (47)
HemoglobinBibba or a2136Pro2, an unstable a chain abnormal hemoglobin (1968) (46)
Radioimmunoassay for abnormal hemoglobins. (1977) (46)
Distal CCAAT box deletion in the A gamma globin gene of two black adolescents with elevated fetal A gamma globin. (1988) (45)
Hemoglobin Louisville (beta-42 (CD1) phe-leu): an unstable variant causing mild hemolytic anemia. (1971) (45)
Studies on the Proportion and Synthesis of Haemoglobin G Philadelphia in Red Cells of Heterozygotes, a Homozygote, and a Heterozygote for both Haemoglobin G and α Thalassaemia (1976) (44)
Properties and inheritance of the new fast hemoglobin type found in umbilical cord blood samples of Negro babies. (1960) (44)
Oxygen equilibria studies of the hemoglobins from normal and anemic sheep and goats. (1968) (44)
One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain. (1989) (43)
Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion. (1977) (42)
The structure of goat hemoglobins. 3. Hemoglobin D, a beta chain variant with one apparet amino acid substitution (21 Asp--His). (1968) (42)
Beta-thalassemia due to a T----A mutation within the ATA box. (1988) (42)
Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. (1992) (42)
Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulation. (1998) (41)
The Use of Globin Chain Electrophoresis in Polyacrylamide Gels for the Quantitation of the Gγ to Aγ Ratio in fetal Hemoglobih (1981) (40)
Hematological observations on Arabian SS patients with a homozygosity or heterozygosity for a beta S chromosome with haplotype #31. (1985) (40)
Detection of common deletional alpha-thalassemia-2 determinants by PCR. (1994) (40)
The G→A Mutation at Position +22 31 to the Cap Site of the β-Globin Gene as a Possible Cause for a β-Thalassemia (1991) (40)
New aspects of the structure, function, and synthesis of hemoglobins. (1970) (40)
Association of the level of G gamma chain in the fetal hemoglobin of normal adults with specific haplotypes. (1986) (39)
International Hemoglobin Information Center. Variant list. (1995) (39)
The production of hemoglobin C in sheep carrying the gene for hemoglobin A: hematologic aspects. (1966) (39)
Variability in the fetal hemoglobin level of the normal adult (1996) (38)
A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis. (1975) (38)
Reverse dot-blot detection of the African-American beta-thalassemia mutations. (1995) (38)
Abnormal arrangements in the alpha- and gamma-globin gene clusters in a relatively large group of Japanese newborns. (1986) (37)
The heterogeneity of goat hemoglobin: evidence for the existence of two nonallelic and one allelic alpha chain structural genes. (1967) (37)
STUDIES ON THE HETEROGENEITY OF HEMOGLOBIN. 8. CHROMATOGRAPHIC AND ELECTROPHORETIC INVESTIGATIONS OF VARIOUS MINOR HEMOGLOBIN FRACTIONS PRESENT IN NORMAL AND IN VITRO MODIFIED RED BLOOD CELL HEMOLYSATES. (1965) (37)
Rickets and amino-aciduria. (1952) (37)
Hb Monroe or alpha 2 beta 230(B12)Arg----Thr, a variant associated with beta-thalassemia due to A G----C substitution adjacent to the donor splice site of the first intron. (1989) (37)
Upstream promoter mutation associated with a modest elevation of fetal hemoglobin expression in human adults. (1988) (37)
Qunatitative determination of the minor hemoglobin component Hb-A2 by DEAE-cellulose chromatography. (1961) (37)
Hemoglobin Savannah (B6(24) β-glycine→valine): an unstable variant causing anemia with inclusion bodies (1971) (36)
An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene. (1989) (36)
An approximately 300 bp deletion involving part of the 5' beta-globin gene region is observed in members of a Turkish family with beta-thalassemia. (1987) (35)
Polymorphisms in the human haptoglobin gene cluster: chromosomes with multiple haptoglobin-related (Hpr) genes. (1986) (35)
Amino-aciduria in rachitic children. (1953) (35)
The two hemoglobin components of the chicken. (1958) (35)
Qualitative and quantitative studies of sickle cell hemoglobin in homozygotes and heterozygotes. (1968) (35)
Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patient. (1989) (34)
Sickle cell anemia as a syndrome: A review of diagnostic features (1979) (34)
Dominant β‐thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the β‐globin gene (1991) (34)
Specific radioimmunochemical identification and quantitation of hemoglobins a2 and f (1976) (34)
Amino aciduria and ascorbic acid deficiency. (1954) (33)
A C----G mutation at nt position 6 3' to the terminating codon may be the cause of a silent beta-thalassemia. (1991) (33)
A laboratory manual on abnormal haemoglobins (1968) (33)
Spleen in sickle cell anemia: Comparative studies of Nigerian and U.S. patients (1993) (32)
SEROLOGIC INVESTIGATIONS OF HUMAN HEMOGLOBINS. II. ANTIBODIES PRODUCED BY ISOLATED HUMAN HEMOGLOBIN TYPES WITH KNOWN STRUCTURAL DIFFERENCES. (1964) (32)
Hereditary persistence of fetal hemoglobin or (delta beta)o-thalassemia: three types observed in South-Chinese families. (1985) (32)
The structure of goat hemoglobins. IV. A third beta chain variant (betaE) with three apparent amino acid substitutions. (1970) (32)
The Thalassemia Repository (Ninth Edition; Part II) (1998) (32)
Structural Characterization of Two δ Chain Variants HEMOGLOBIN A'2 (B2) AND HEMOGLOBIN FLATBUSH (1967) (32)
Hb Lepore-Baltimore (δ68Leu-β84Thr) and Hb Lepore-Washington-Boston (δ87Gln-βIVS-II-8) in Central Portugal and Spanish Alta Extremadura (1997) (31)
An electronic database of human hemoglobin variants on the World Wide Web. (1998) (31)
High frequencies of a rearrangement (+ATA; -T) at -530 to the beta-globin gene in different populations indicate the absence of a correlation with a silent beta-thalassemia determinant. (1989) (31)
THE STRUCTURE OF SHEEP HEMOGLOBINS. THE AMINO ACID COMPOSITIONS OF THE ALPHA AND BETA CHAINS OF THE HEMOGLOBINS, A, B, AND C. (1965) (31)
Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes. (1991) (31)
β-thalassemia in Bulgaria (1990) (30)
Heterogeneity of fetal hemoglobin in beta-thalassemia of the Negro. (1970) (30)
Further Studies of the Postnatal Change in Chemical Heterogeneity of Human Fetal Hemoglobin in Several Abnormal Conditions (1975) (30)
Characterization of Three Types of β0-Thaussemia Resulting from a Partial Deletion of the β-Globin Gene (1989) (30)
An improved chromatographic procedure for quantitation of human fetal hemoglobin. (1977) (30)
Two Independent Genetic Factors in the j9-Globin Gene Cluster Are Associated With High G7..Levels in the HbF of SS Patients (1984) (30)
The β- and δ-Thalassemia Repository (Seventh Edition) (1993) (29)
Investigations on two different hemoglobins of the sheep. (1957) (29)
Hemoglobin Istanbul: substitution of glutamine for histidine in a proximal histidine (F8(92) ). (1972) (29)
Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β‐thalassaemia due to a homozygosity for the IVS‐I‐6 (T→C) mutation (1994) (29)
Hemoglobin Grady: the first example of a variant with elongated chains due to an insertion of residues. (1974) (29)
Chromatographic separation of hemoglobins A 2 and C. The quantities of hemoglobin A 2 in patients with AC trait, CC disease, and C- -thalassemia. (1972) (28)
Certain mutations observed in the 5' sequences of the G gamma- and A gamma-globin genes of beta S chromosomes are specific for chromosomes with major haplotypes. (1991) (28)
A comparative study of enzymic activities in normal adult and cord blood erythrocytes as related to the reduction of methemoglobin (1962) (28)
COMPARATIVE STUDIES OF OXYGEN EQUILIBRIA OF HUMAN ADULT AND CORD BLOOD RED CELL HEMOLYSATES AND SUSPENSIONS. (1964) (28)
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations. (1992) (28)
The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C----G substitution at nucleotide -195 of the A gamma-globin gene. (1990) (27)
Further modification of the microchromatographic determination of hemoglobin A2. (1977) (27)
The Haemoglobins of Sheep (1975) (27)
Combinations of β chain abnormal hemoglobins with each other or with β-thalassemia determinants with known mutations: influence on phenotype (1997) (27)
An ~300 bp deletion involving part of the 5' β-globin gene region is observed in members of a Turkish family with β-thalassemia (1987) (27)
A novel deletion of approximately 27 kb including the beta-globin gene and the locus control region 3'HS-1 regulatory sequence: beta zero-thalassemia or hereditary persistence of fetal hemoglobin? (1994) (27)
The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene. (1991) (27)
STUDIES ON ANIMAL HEMOGLOBINS. 3. THE POSSIBLE ROLE OF INTERCELLULAR INORGANIC PHOSPHATE ON THE OXYGEN EQUILIBRIUM OF THE HEMOGLOBIN IN THE DEVELOPING CHICKEN. (1964) (27)
Low pulse oximeter‐measured hemoglobin oxygen saturations with hemoglobin Cheverly (1998) (27)
Anomaly in the γ chain heterogeneity of the newborn (1977) (27)
Hemoglobin G Georgia or α295 Leu (G-2) β2 (1970) (26)
Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the Gγ and Aγ types of γ chain (1984) (26)
The chromatographic behaviour of different abnormal human haemoglobins on the cation exchanger amberlite IRC 50. (1957) (26)
Chromatographic Estimation of Different Kinds of Human Hæmoglobin (1955) (26)
Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs. (1994) (26)
Two novel polyadenylation mutations leading to beta(+)-thalassemia. (1990) (26)
Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populations. (1993) (26)
α‐Thalassemia and β‐thalassemia in a turkish family (1977) (26)
Haemoglobin α Chain Duplication in Barbary Sheep, Ammotragus lervia, Pallas, 1777 (1970) (26)
Another form of the hereditary persistence of fetal hemoglobin (the Atlanta type)? (1976) (25)
The Structure of Sheep Hemoglobins III. STRUCTURAL STUDIES OF THE α CHAIN OF HEMOGLOBIN A (1968) (25)
γ Chain Abnormalities and γ-Globin Gene Rearrangements in Newborn Babies of Various Populations (1991) (25)
Normal fetal hemoglobin levels in the sudden infant death syndrome. (1989) (25)
Amino acid sequences in the -chains of adult bovine hemoglobins C-Rhodesia and D-Zambia. (1972) (25)
Hemoglobin α Chain Deficiency in Black Children with Variable Quantities of Hemoglobin Bart's at Birth (1977) (25)
Sheep hemoglobin D, an α-chain variant with one apparent amino acid substitution (α 15 Gly →Asp) (1968) (25)
A possible subclass of the hereditary persistence of fetal hemoglobin. (1970) (25)
Subunit dissociation of the abnormal hemoglobins G Georgia ( 2 95Leu (G2) 2 ) and Rampa ( 2 95Ser (G2) 2 ). (1972) (24)
Further studies on the quantitation of the hemoglobins A, S, C, and F in newborn babies with different hemoglobinopathies using high pressure liquid chromatography. (1982) (24)
Heterogeneity of fetal hemoglobin in β-thalassemia of the Negro. (1970) (24)
Non-synchronized suppression of postnatal activity in non-allelic genes which synthesize the Ggamma chain in human foetal haemoglobin. (1973) (24)
Gene deletion as the molecular basis for the Kenya-G gamma-HPFH condition. (1983) (24)
β‐thalassemia alleles and unstable hemoglobin types among russian pediatric patients (1994) (24)
Black β‐thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site‐2 of the locus control region have high levels of fetal hemoglobin (1992) (23)
Difference in Gross Structure of Two Electrophoretically Identical ‘Minor’ Hæmoglobin Components (1962) (23)
The quantities of various minor hemoglobin components in old and young human red blood cells. (1967) (23)
Studies on a fast hemoglobin variant found in a negro family in association with thalassemia (1961) (23)
Beta-thalassemia in four Mediterranean countries; an editorial commentary. (1990) (23)
Analysis of hemoglobin F production in Saudi Arabian families with sickle cell anemia. (1987) (23)
Microchromatography of hemoglobins. IV. An improved procedure for the detection of hemoglobins S and C at birth. (1975) (23)
The beta- and delta-thalassemia repository. (1992) (23)
The chemical heterogeneity of human hemoglobin F: Direct evidence for the existence of three types of γ chain, the GγI, AγI, and AγT chains (1979) (22)
Studies of haemoglobin types in barbary sheep (Ammotragus lervia). (1968) (22)
Hemoglobin beograd or α2β2121 Glu→Val (GH4) (1973) (22)
A Second Type of Hereditary Persistence of Foetal Haemoglobin in India (1973) (22)
Hemoglobin Russ oor α251argβ2 (1966) (22)
Is foetal haemoglobin present in the blood of normal human adults? (1955) (22)
The concentration of different amino acids in the blood plasma in children suffering from rickets and scurvy. (1954) (21)
Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants. (1972) (21)
Beta zero-thalassemia in association with a gamma-globin gene quadruplication (1986) (21)
The 18- to 23-kb deletion of the Macedonian delta beta-thalassemia includes the entire delta and beta globin genes. (1986) (21)
Minor hemoglobins in sickle-cell heterozygotes and homozygotes with and without diabetes. (1980) (21)
The hemoglobin heterogeneity of the Virginia white-tailed deer: a possible genetic explanation. (1968) (21)
Molecular heterogeneity of beta-thalassemia intermedia in Turkey. (1989) (21)
Two new large deletions resulting in εγδβ-thalassemia (1988) (21)
Hb Alesha or alpha 2 beta (2)67(E11)Val-->Met: a new unstable hemoglobin variant identified through sequencing of amplified DNA. (1993) (21)
Homozygous hemoglobin O Arab in a gypsy family in Yugoslavia. (1977) (21)
Distribution of beta-thalassemia mutations in three Asian Indian populations with distant geographical locations. (1994) (21)
Homozygous beta0- and beta+ - thalassemia in Kurdish Jews and Arabs. (1977) (20)
The gamma chain heterogeneity of fetal hemoglobin in black beta-thalassemia and HPFH heterozygotes. (1981) (20)
Hb A2-Wrens or α2δ298(FG5)Val → MEt, an unstable δ chain variant identified by sequence analysis of amplified DNA (1989) (20)
Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure (1988) (20)
A novel α‐thalassemia‐2 (−2.7‐kb) observed in a chinese patient with Hb H disease (1991) (20)
One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population (1987) (20)
Detection of the embryonic ζ chain in blood from newborn babies by reversed-phase high-perfomance liquid chromatogrphy (1987) (20)
Hb Leslie, an unstable hemoglobin due to deletion of glutaminyl residue beta 131 (H9) occurring in association with beta0-thalassemia, HbC, and HbS. (1976) (20)
Genetic heterogeneity of β‐thalassemia in southeast sicily (1995) (20)
STUDIES ON ANIMAL HEMOGLOBINS. II. THE INFLUENCE OF INORGANIC PHOSPHATE ON THE PHYSICO-CHEMICAL AND PHYSIOLOGICAL PROPERTIES OF THE HEMOGLOBIN OF THE ADULT CHICKEN. (1964) (20)
Analysis of Hemoglobin F Production in Saudi Arabian Families With Sickle Cell Anemia (1987) (19)
β-Thalassehia Repository (1989) (19)
Some characteristic properties of hemoglobin C. (1955) (19)
The Synthesis of Fetal Hemoglobin Types in red Blood Cells and in BFU-E Derived Colonies from Peripheral Blood of Patients with Sickle Cell Anemia, β+- and δβ-Thalassemia, Various forms of Hereditary Persistence of Fetal Hemoglobin, Normal Adults and Newborn (1979) (19)
Studies on the heterogeneity of hemoglobin. XVI. Separation of variants with a GlU-Lys substitution by chromatography on CM-cellulose. (1974) (19)
The oxygen equilibria of some "slow-moving" human hemoglobin types. (1963) (19)
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients. (1993) (18)
A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α2Gγ292(F8)HIS→TYR (1992) (18)
Genetic Aspects of Two Different Minor Hæmoglobin Components found in Cord Blood Samples of Negro Babies (1960) (18)
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia. (1991) (18)
STUDIES ON ANIMAL HEMOGLOBINS. I. HEMOGLOBINS IN TURTLES. (1964) (18)
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site. (1991) (18)
Hemoglobin-strumica or α2112(G19)His→Argβ2. (with an addendum: Hemoglobin-J-paris-I, α212(A10)A1a→Aspβ2, in the same population) (1975) (18)
The types of hemoglobins and globin chains in hydrops fetalis. (1989) (18)
Observations on the Levels of Hb A, in Patients With Different @-Thalassemia Mutations and a 6 Chain Variant (2003) (18)
High performance liquid chromatographic analysis of human hemoglobins and their polypeptide chains: Its use in the identification of variants (1997) (18)
Hemoglobin atlanta or α2β275 Leu→Pro (E19); An unstable variant found in several members of a caucasian family (1975) (18)
Studies on the heterogeneity of hemoglobin. III. The heterogeneity of some animal hemoglobins. (1960) (17)
βthalassemia intermedia in two turkish families is caused by the interaction of HB knossos [β27(b9)ALA→SER] and of HB city of Hope [β69(e13)gly→ser] with b°thalassemia (1989) (17)
Amino-Acid Composition of Adult and Fœtal Myoglobin of the Cow (1957) (17)
Hemoglobin athens-georgia, or α2β240(C6)Arg→Lys, a hemoglobin variant with an increased oxygen affinity (1976) (17)
The sulfhydryl groups of four different human haemoglobins. (1956) (17)
The beta- and delta-thalassemia repository (Ninth Edition; Part I). (1998) (17)
Rapid cation-exchange high-performance liquid chromatographic procedure for the separation and quantitation of hemoglobins S, C, and O Arab in cord blood samples. (1986) (17)
Percentages of abnormal hemoglobins in adults with a heterozygosity for an α‐chain and/or a β‐chain variant (1983) (17)
Hb Doha or α2β2[X-N-Met-1(NA1)Val→Glu]; a new β-chain abnormal hemoglobin observed in a Qatari female (1985) (17)
Hb E and α-Thalassemia; Variability in the Assembly of βE Chain Containing Tetramers (1997) (16)
Haplotypes and alpha globin gene analyses in sickle cell anaemia patients from Kenya. (1987) (16)
Investigations of Molecular Variation in Human Fetal Hemoglobin in the Infant and in Certain Hematological Conditions in the Adult (1970) (16)
The combination of HB S and HB E in a black female. (1976) (16)
Structural studies of hemoglobin chains from Virginia white-tailed deer. (1972) (16)
Hemoglobin A2-indonesia or α2δ269(E13)Gly→Arg (1971) (16)
The dominant β‐thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon (=arginine) at the 5′ end of the second exon (1996) (16)
Co‐Inheritance of Hb D‐PUNJAB (CODON 121; GAA→CAA) and β0-Thalassemia (IVS‐II-1; G→A) (1996) (16)
Gene duplication of the α chain of goat hemoglobin: Evidence from a homozygous mutant (1968) (16)
Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants. (1991) (16)
Molecular Characterization of β-Thalassemia in North Jordan (1994) (16)
The renal element in rachitic amino-aciduria. (1954) (16)
Carboxylmethyl-cellulose microchromatography for the quantitation of hemoglobin Bart's (γ4) and its use in the detection of the α-thalassemia conditions (1980) (15)
The frequency of the γ chain variant AγT in different populations, and its use in evaluating γ gene expression in association with thalassemia (1985) (15)
The chemical heterogeneity of the fetal hemoglobin in normal newborn infants and in adults (1977) (15)
The Structure of Goat Hemoglobins V. A Fourth β Chain Variant (β-D-Malta; 69 Asp ↠ Gly) with Decreased Oxygen Affinity and Occurring at a High Frequency in Malta (1979) (15)
A large beta-thalassemia deletion in a family of Indonesian-Malay descent. (1996) (15)
LINKAGE OF THE BETA-CHAIN AND DELTA-CHAIN STRUCTURAL GENES OF HUMAN HEMOGLOBINS. (1963) (15)
An Unusual Hemoglobin Anomaly and Its Relation to α-Thalassemia and Hemoglobin-H Disease (1971) (15)
Separation of the Aγ and Gγ cyanogen bromide peptides of human fetal hemoglobin by high-pressure liquid chromatography (1979) (15)
Hb Hradec Kralove (Hb HK) or alpha 2 beta 2 115(G17)Ala-->Asp, a severely unstable hemoglobin variant resulting in a dominant beta-thalassemia trait in a Czech family. (1993) (15)
Allele-specific amplification for the identification of several hemoglobin variants. (1993) (15)
Microchromatographic quantitation of fetal hemoglobin in patients with sickle cell disease. (1979) (15)
Haplotype-specific sequence variations in the locus control region (5' hypersensitive sites 2, 3, 4) of beta S chromosomes. (1993) (15)
Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin gene. (1990) (15)
Hemoglobin St Luke's or α95Arg2 (G2) β2 (1972) (15)
Beta-thalassemia in Turkey. (1990) (15)
Hb Graz or α2β22(Na2)His→Leu; a new β Chain Variant Observed in four Families from Southern Austria (1992) (14)
Hb CAPA OR α2 94(G1)ASP→GLYβ2, A Mildly Unstable Variant with an A↠G (Gac↠Ggc) Mutation in Cown 94 of the α1-Globin Gene (1994) (14)
Hb E and Hb E-like variants in individuals from Turkey. (1981) (14)
The identification of five rare beta-chain abnormal hemoglobins by high performance liquid chromatographic procedures. (1986) (14)
Some Investigations on the Metabolism of Phenylalanine and Tyrosine in Children with Vitamin C Deficiency (1957) (14)
The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes. (1984) (14)
alpha-Thalassaemia in the population of Cyprus. (1995) (14)
Alternate organization of alpha G-Philadelphia globin genes among U.S. black and Italian Caucasian heterozygotes. (1984) (14)
Hydrops fetalis due to homozygosity for α-thalassemia-1, -(α)-20.5.kb: the first observation in a turkish family (1989) (14)
The heterogeneity of the gamma-chain of fetal hemoglobin in HbS heterozygotes. (1982) (14)
Hemoglobin Köln in a black: pre- and post-splenectomy red cell survival (DF32P and 51Cr) and the pathogenesis of hemoglobin instability. (1973) (14)
Trimodality in the percentages of beta chain variants in heterozygotes: the effect of the number of active Hbalpha structural loci. (1977) (14)
Hemoglobin Jenkins or hemoglobin-N-Baltimore or α2β295Glu (1966) (14)
A Case of Hæmoglobin J in an Indonesian Family (1957) (14)
The action of carboxypeptidase on different human haemoglobims. (1956) (13)
In vitro synthesis of hemoglobin and hemoglobin chains in the BFUe-derived colonies form person with alpha- or beta-thalassemia. (1981) (13)
Variability in the interaction of beta-thalassemia with the alpha-chain variants Hb G-Philadelphia and Hb Rampa. (1978) (13)
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adult. (1990) (13)
Hb Wuming or alpha 2 11(A9)Lys substituting for Gln beta 2. (1981) (13)
Hemoglobinopathies observed in the population of the Southeastern United States (SE-USA). (1980) (13)
HB F-Tokyo or α2Gγ234 (B16) val→ile, a silent γ chain variant detected by reverse phase high performance liquid chromatography (1985) (13)
Hemoglobin Montreal: a new variant with an extended beta chain due to a deletion of Asp, Gly, Leu at positions 73, 74, and 75, and an insertion of Ala, Arg, Cys, Gln at the same location. (1991) (13)
Hb-Alberta or α2β2 (101(G3) GLU→GLY), a New High-Oxygen-Affinity Hemoglobin Variant Causing Erythrocytosis (1976) (13)
Some properties of hemoglobin Gun Hill. (1977) (13)
Level of fetal hemoglobin in children with sickle cell anemia: influence of gender, haplotype and alpha-thalassemia-2 trait. (1993) (13)
Molecular characterization of Hb S(C) beta-thalassemia in American blacks. (1991) (13)
Hemoglobin fort gordon or α2β2145 Tyr → Asp, a new high-oxygen-affinity hemoglobin variant (1975) (13)
Hb F in sickle cell anemia (1993) (13)
The separation of human hemoglobin chains by high pressure liquid chromatography. (1981) (13)
Studies on the heterogeneity of hemoglobin : XV. Separation of fetal hemoglobin and the normally occurring minor adult hemoglobins by chromatography on DEAE-cellulose (1974) (12)
The production of haemoglobin C in adult sheep and goats. (1969) (12)
Chinese in west Malaysia: the geography of beta thalassaemia mutations. (1990) (12)
Evidence for four nonallelic structural genes for the γ chain of human fetal hemoglobin (1972) (12)
Four categories of gamma-globin gene triplications: DNA sequence comparison of low G gamma and high G gamma triplications (1988) (12)
Some rare hemoglobin variants with altered oxygen affinities; Hb linkoping [beta 36(C2)Pro----Thr], Hb Caribbean [beta 91(F7)Leu----Arg], and Hb Sunnybrook [beta 36(C2)Pro----Arg]. (1988) (12)
The alpha / beta and alpha 2 / alpha 1-globin mRNA ratios in different forms of alpha-thalassemia. (1996) (12)
Hb Bab-Saaooun or α2β248(CD7)Leu→pro, A Mildly Unstable Variant Found in an Arabian Boy from Tunisia (1992) (12)
HB Extremadura or α2β2133(H11)VAU→LEU, A New Mildly Unstable Hemoglobin in a Spanish Female (1989) (12)
A Short Review of Human γ-Globin Gene Anomalies (1987) (12)
On the structure of the hemoglobins A, A2, and F in a Negro with homozygous beta-thalassemia. (1974) (12)
Studies on the heterogeneity of hemoglobin. XI. Chromatographic studies of intermediate forms of oxy- and ferrihemoglobin. (1966) (12)
Delta beta-thalassemia in a Mexican family: clinical differences among homozygotes. (1978) (12)
Quantitation of hemoglobins Bart's, H, Portland-I, Portland-II and constant spring by anion-exchange high-performance liquid chromatography. (1989) (12)
Hb S, Hb G-PHILADELPHIA AND α-THALASSEMIA-2 IN A BLACK FAMILY (1980) (12)
Hb-volga or α2β227(B9)Ala→Asp an unstable hemoglobin variant in three generations of a dutch family (1976) (12)
Subunit Dissociation of the Unstable Hemoglobin Bibba (α2136 pro (H19)β2) (1970) (12)
The heterogeneity of the fetal hemoglobin of the goat. (1969) (12)
Microchromatography of hemoglobins : VII. Detection of some uncommon hemoglobin variants and two rapid methods for the quantitation of Hb-A2 in the presence of Hb-C (1977) (12)
The Unstable HB Hammersmith or α2β242(CD1)PHE→SER Observed in an Indian Child; Identification by HPLC AND by Sequence Analysis of Amplified DNA (1992) (11)
The characterization of variants of human hemoglobin A2. (1974) (11)
Some physicochemical properties of hemoglobin-manitoba (α2102Ser → Arg(G9)β2) (1975) (11)
Investigations on heat-coagulable globulin in the blood of a patient with multiple myeloma. (1956) (11)
Serological investigations of some human and animal hemoglobins by the agar gel-diffusion method. (1960) (11)
The Determination of the Percentages of Gγ and Aγ Chains in Human Fetal Hemoglobin by HPLC (1980) (11)
Transient chloramphenicol acetyltransferase expression of the G gamma globin gene 5'-flanking regions containing substitutions of C----T at position -158, G----A at position -161, and T----A at position -175 in K562 cells. (1989) (11)
A new "fast" hemoglobin found in umbilical cord blood of Negro babies. (1960) (11)
HB Coimbra or α2β299(Gl)ASP→GLU, A Newly Discovered High Oxygen Affinity Variant (1991) (11)
A new abnormal human hemoglobin-Hb: Zurich. (1961) (11)
Posttranslational Modification of β141 LEU Associated with the β75(E19)Leu→pro Mutation in HB Atlanta (1993) (11)
A de novo Deletion Causing εγδβ-Thalassemia in a Dutch Patient (1996) (11)
Haemoglobin M Saskatoon and haemoglobin M Hyde Park in two Yugoslavian families. (2009) (11)
Production of hemoglobin C in the Moufflon (Ovis musimon pallas, 1811) and the Barbary sheep (Ammotragus lervia pallas, 1777) during experimental anemia: Amino acid composition of tryptic peptides from the βB and βC chains (1970) (11)
The N-terminal residues of five different human haemoglobins. (1955) (11)
Experiences with the quantitation of human hemoglobin types by high pressure liquid chromatography. (1981) (11)
Hemoglobin Types in Barbary Sheep (Ammotragus Lervia Pallas, 1777) Absence of a βc Production in a Homozygous βc(na) Animal During Severe Anemia 1 (1972) (10)
Hb Setif or alpha 2 94(G1)Asp----Tyr beta 2 observed in a Saudi Arabian family. (1985) (10)
Binding of nuclear factors to the proximal and distal CACCC motifs of the beta-globin gene promoter: implications for the -101 (C-->T) 'silent' beta-thalassemia mutation. (1994) (10)
Haplotypes among Vietnamese hemoglobin E homozygotes including one with a gamma-globin gene triplication. (1986) (10)
A Fetal Hemoglobin with Abnormal γ-Polypeptide Chains: Hemoglobin Warren (1965) (10)
Hb Le Lahentin or α220(B1)His→Glnβ2 Found in a Spanish Family (2009) (10)
Hb F-M-Osaka or alpha 2G gamma 2(63)(E7)His----Tyr in a Caucasian male infant. (1989) (10)
Hb Oloc or α2β286(F2)Ala → Asp, A New High Oxygen Affinity Variant (1987) (10)
Co-inheritance of Hb D-Punjab (codon 121; GAA-->CAA) and beta (0) -thalassemia (IVS-II-1;G-->A). (1996) (10)
Hb lulu island (α2β2107[G9]Gly→Asp)‐β°‐thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia (1995) (10)
Hb F-Charlotte, an Aγ Variant with a Threonine Residue in Position γ75 and a Glycine Residue in Position γ136 (1990) (10)
Detection of alpha-thalassemia-2 (-3.7 kb) and its corresponding triplication (alpha)(alpha)(alpha) (anti-3.7 kb) by PCR: an improved technical change. (1996) (10)
A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His----Tyr. (1992) (10)
Hemoglobin Hamadan or α2β256(D7)Gly→Arg in a Turkish Family (1984) (10)
Heterozygosity and Homozygosity for the High Oxygen Affinity Hemoglobin Tarrant or α126 (H9) ASP→ASN in two Mexican Families (1981) (10)
Post-translational control of human hemoglobin synthesis; the number of alpha chain genes and the synthesis of HB S. (1978) (10)
Frequency of the alpha-thalassemia-2 gene among Nigerian SS patients and its influence on malaria antibody titers. (1993) (10)
Haemoglobin types in different species of sheep. (1958) (10)
A chromosome with five gamma-globin genes. (1988) (10)
Hb Beograd-beta zero thalassemia in a Turkish family from Yugoslavia. (1984) (10)
Homozygosity for a New Type of Gγ(Aγδβ)°-Thalassemia in a Malaysian Male (1986) (10)
Excretion of amino acids in free and bound form during intravenous administration of protein hydrolysate. (1957) (10)
Hb J-Antakya or α2β265(E9)Lys → Met in a Turkish family and Hb Complutense or α2β2127(H5)Gln → Glu in a Spanish family; correction of a previously published identification (1986) (10)
Analysis of mRNA from red cells of patients with thalassemia and hemoglobin variants. (1997) (10)
Hemoglobin Hofu or αβ [126 (H4) Val → Glu] Found in Combination with Hemoglobin S (1978) (10)
Adult and fetal hemoglobin production in erythroid colonies from subjects with beta-thalassemia or with hereditary persistance of fetal hemoglobin (HPFH). (1980) (10)
HB Mizuho or α2β268(E12)Leu→pro in a Caucasian Boy with high levels of HB F; Identification by Sequencing of Amplified DNA (1991) (10)
Some investigations dealing with animal haemoglobins. (1958) (10)
Hb Camden and Hb Hope found during routine testing. (1975) (10)
Application of high-performance liquid chromatographic methodology to the analysis of hemoglobins synthesized in erythroid progenitor cells. (1989) (9)
Factors Associated With Hypochromia and Microcytosis Among High School Students in the Southeastern United States (1994) (9)
Some notes about Hb Q-India and Hb Q-Iran. (1986) (9)
Hb Tigraye or alpha 2 beta (2)79(EF3)Asp-->His(GAC-->CAC): a hemoglobin variant with increased oxygen affinity observed in an Ethiopian male. (1993) (9)
New ultra-micro high-performance liquid chromatographic method for determining the gamma chain composition of hemoglobin F in normal adults. (1993) (9)
Hb-Genova (α2β228(bio)leu→pro); methods for detection and analysis of unstable hemoglobins (1973) (9)
Some genetic and physiological aspects of two different adult haemoglobins in sheep. (1958) (9)
Thalassemia intermedia caused by heterozygosity for both β‐thalassemia and hemoglobin saki [β14 (a11) leu→pro] (1976) (9)
Detection of a new hybrid α2 globin gene among American Blacks (1988) (9)
Hb Iowa or α2β2119(GH2)GLY→ALA (1990) (9)
The Influence of Antiserum to Human Erythropoietin on the Production of Hemoglobin C in Goats 1 (1970) (9)
Hb natal or α2(minus Tyr-Arg)β2: a high oxygen affinity α chain variant with a deleted carboxy-terminus resulting from a TAC → TAA (Tyr→ terminating codon) mutation in codon α140 (1988) (9)
HB Duan [α75(EF4)ASP→ALA), HB Westmead [α122(H5)HIS→GLN], and α-Thalassemia-2 (-4.2 KB Deletion) in a Chinese Family (1988) (9)
Hydroxyurea therapy in sickle cell anemia patients in Curaçao, The Netherlands Antilles. (1997) (9)
Minor hemoglobins (Hb AI) in chronic alcoholic patients. (1982) (9)
Usefulness of HPLC methodology for the characterization of combinations of the common β chain variants HBS s, c, and o-ARAB, and the α chain variant HB g-philadelphia (1993) (9)
Hb Las Palms or α2β249(Cd8)Ser→Phe, a Mildly Unstable Hemiglobin Variant (1988) (9)
HB Vaasa or α2β2(39(C5)CLN→GLU), A Mildly Unstable Variant Found in a Finnish Family (1977) (9)
Evidence of a Second Fœtal Hæmoglobin in the Newborn Goat (1957) (9)
Hemoglobin Handsworth or α218(A16)Gly→Argβ2 in a Saudi Newborn (1985) (9)
A newly discovered frameshift at codons 120-121 (+A) of the beta gene is not associated with a dominant form of beta-thalassemia. (1996) (9)
Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major. (1989) (9)
Newer developments in the identification of beta-thalassemia. (1988) (9)
Adult hemoglobin levels in newborn babies from different countries and in babies with some significant hemoglobinopathies. (1987) (9)
Hb F-Forest Park, a new A gamma variant with two amino acid substitutions, 75(E19)Ile----Thr and 73(E17)Asp----Asn, which can be identified in adults by gene-mapping analysis. (1985) (9)
A second family with the Atlanta type of HPFH. (1985) (9)
A Canadian family with Hb Wayne; characterization by HPLC and DNA sequencing. (1992) (9)
Normal and abnormal human hemoglobins. (1972) (9)
Dutch beta 0-thalassaemia: a 10 kilobase DNA deletion associated with significant gamma-chain production. (1984) (9)
An IVS-I-117 (G-->A) acceptor splice site mutation in the alpha 1-globin gene is a nondeletional alpha-thalassaemia-2 determinant in an Indian population. (1993) (9)
Hb Wayne, the frameshift variant with extended alpha chains observed in a Caucasian family from Alabama. (1984) (9)
Hemoglobins A 2 -Sphakiá and A 2 -NYU in Canada. (1972) (9)
Hemoglobin Louisville (beta 42 (CD1) phenylalanine replaced by leucine) occurring as a fresh mutation in a Canadian woman. (1978) (8)
Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: beta 111 GTC-->CTC (Val-->Leu) and beta 119 GGC-->GAC (Gly-->Asp). (1994) (8)
Abnormal γ-Globin Gene Arrangements in Sardinians (1988) (8)
Observations on the calculated contents of variant and normal alpha chains in adult and fetal erythrocytes. (1979) (8)
HB Beth Israel (β102 [G4] ASN → SER) Observed in a Yugoslavian Teenager (1978) (8)
A Newly Discovered β°-Thalassemia (IVS-11-850, G→A) Mutation in a North European Family (1995) (8)
Variations in Gγ, and Aγ Ratios in the Fetal Hemiglobin of Newborn Babies (1988) (8)
The levels of zeta, gamma, and delta chains in patients with Hb H disease. (1989) (8)
Characterization of Abnormalities in the γ-Globin Gene Arrangements of Japanese Newborns (1988) (8)
The Characterization of Hemoglobin Manitoba or α2102(G9)Ser→Argβ2 and Hemoglobin Contaldo or α2103(G10)HIS→ARGβ2 By High Performance Liquid Chromatography (2009) (8)
Geographic distribution of hemoglobin variants in the white-tailed deer. (1973) (8)
Hb Himeji or α2β2140(h18)ala→asp in a portuguese family (1989) (8)
Characterization of the beta+-thalassemia mutation in a homozygous Yugoslavian patient. (1984) (8)
Incorrect genetic counseling of a couple with beta-thalassemia, due to incomplete testing. (1993) (8)
HB Cleveland or α2β293(F9)CYS→ARG;121(GH4)GLU→GLN (1991) (8)
Radioimmunochemical characterization of hemoglobins Lepore and Kenya: unique antigenic determinants located on hybrid hemoglobins. (1978) (8)
beta S-haplotypes and alpha-thalassemia along the coastal belt of Kenya. (1989) (8)
The usefulness of sequence analysis of amplified DNA for the identification of delta chain variants. (1991) (8)
Saudi Arabian Sickle Cell Anemia a (1989) (8)
Haemoglobin Presbyterian [beta 108 (G 10) Asn----Lys] in a Spanish family. (1986) (8)
Hb F-Marietta or GγI 80[EF4] ASP à Asn, Observed in a Caucasian Baby (1982) (8)
Hb A2-Canada or alpha 2 delta 2 99(G1) Asp replaced by Asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia. (1982) (8)
A 2nd, Elongated, α-2-Globin m-RNA Is Present in Reticulocytes from Normal Persons and Subjects with Terminating Codon or Poly A Mutations (1995) (8)
Molecular packing and intermolecular contacts of sickling deer type III hemoglobin. (1979) (8)
The postnatal synthesis of fetal hemoglobin. I. Some studies in newborn goats using radioactive Fe59 and glycine-2-C14. (1957) (8)
Molecular characterization of beta-thalassemia in Hungary. (1993) (7)
Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta-thalassemia trait. (1994) (7)
Globin mRNA in β-thalassemia heterozygotes with different β-thalassemia alleles and in heterozygotes for hereditary persistence of fetal hemoglobin (1996) (7)
The relative levels of α2-, α1-, and ζ-mRNA in HB H patients with different deletional and nondeletional α-thalassemia determinants (1996) (7)
A second, elongated, alpha 2-globin mRNA is present in reticulocytes from normal persons and subjects with terminating codon or poly A mutations. (1995) (7)
Heterogeneity of fetal hemoglobin among Israel families with beta-thalassemia. (1973) (7)
A novel alpha-thalassemia-2 (-2.7-kb) observed in a Chinese patient with Hb H disease. (1991) (7)
The DNA deletion in an Indian delta beta-thalassaemia begins one kilobase from the A gamma globin gene and ends in an L1 repetitive sequence. (1989) (7)
Nonallelic structural genes and hemoglobin synthesis. (1970) (7)
Haemoglobin types in pre- and postnatal life (1959) (7)
Amino-acid Composition of Hæmoglobin E (1956) (7)
Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels. (1992) (7)
Hb P-Nilotic in association with beta0-thalassemia: cis-mutation of a hemoglobin betaA chain regulatory determinant? (1979) (7)
HB Mizuho or α2β268(E12)LEU→PRO in a Young Dutch Boy (1995) (7)
HB Nottingum or α2β298(F65)VAL→GLY Observed as a De Novo Mutation in a Canadian Child (1992) (7)
An initiation codon mutation as a cause of a beta-thalassemia. (1990) (7)
Hb A2-Manzanares Or α2δ2 121(Gh4) Glu→Val, An Unstable δ Chain Variant Observed in a Spanish Family (1983) (7)
Haplotypes in SS patients from Nigeria; characterization of one atypical βS haplotype no. 19 (Benin) associated with elevated HB F and highGγ levels (1992) (7)
[Studies on abnormal hemoglobin c]. (1955) (7)
Hb Nottingham (α;2β;2 (FG5) 98 VAL→GLY) in a Caucasian male : clinical and biosynthetic studies (1978) (7)
Hemoglobin St Luke's, or alpha 2 , 95 Arg (G2) beta 2 . (1972) (7)
Hb F-Kennestone or α2Gγ2 (EF1)77 His → Arg Observed in a Caucasian Baby (1983) (7)
Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia. (1994) (7)
Multiple α and β Chain Structural Genes as a Basis for Hemoglobin Heterogeneity of the Adult Goat (1970) (7)
β-Thalassemia Intermedia in An Indian Female h the Hb Hofu [β126(H4)Val→Glu]-(β°-Thalassemia [Codons 8/9 (+G)] Combination (1995) (7)
Fetal hemoglobin in normal adults and beta-thalassemia heterozygotes. (1990) (7)
Hb Cheverly or alpha 2 beta 2 45(CD4)Phe replaced by Ser in an elderly Italian male. (1982) (7)
Effect of Severe Hemorrhage on the Hemoglobins of a Virginian White-Tailed Deer (Odocoileus virginianus)∗ (1968) (7)
Identification of Several α-Globin Gene Variations in a Small Laotian Family (1995) (7)
Hb F-LA grange or α2γ2101(G3)Glu → Lys; 75IIe; 136Gly: A high affinity fetal hemoglobin variant observed in a caucasian newborn (1984) (7)
Further studies on the cysteine-cystine content of the foetal-human haemoglobin. (1958) (7)
The β-δ crossover leading to the βδ hybrid gene of hemoglobin P-Nilotic is located within 54 base-pairs of the 5′ end of exon 2 or between codons 31 and 50 (1987) (7)
SLIGHT INCREASE OF FETAL HEMOGLOBIN IN APPARENTLY HEALTHY NEGROES. (1965) (7)
Absence of Abnormal Hæmoglobins in Some Groups of the Papua Population of Dutch New Guinea (1958) (7)
HB P-Nilotic or α2(βδ)2 in a Turkish Family (1987) (7)
The structure of sickling deer type III hemoglobin by molecular replacement (1977) (7)
Hb H disease and mild mental retardation in a black girl with a Hb S heterozygosity. (1992) (6)
The distribution of fetal hemoglobin and the types of gamma chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies. (1983) (6)
Comparison of the Relative Quantities of γ-mRNAs and Fetal Hemoglobin in SS Patients with Different Haplotypes (1998) (6)
HB Hakkari or α2β231(B13)LEU→ARG, A Severely Unstable Hemoglobin Variant Associated with Numerous Intra-Erythroblastic Inclusions and Erythroid Hyperplasia of the Bone Marrow (1995) (6)
Hb Capa or alpha (2)94(G1)Asp-->Gly beta 2, a mildly unstable variant with an A-->G (GAC-->GGC) mutation in codon 94 of the alpha 1-globin gene. (1994) (6)
A New Slow-Moving Hemoglobin Variant Hb Tiani or α2β239(C5)Gln+Arg, Observed In A Chinese Family Living In Gansu (1990) (6)
Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chain. (1984) (6)
Identification of hemoglobin G-Philadelphia (α68 Asn→Lys) and homoglonin matsue-oki (α75 Asp→Asn) in a black infant (1982) (6)
A comparative study of some different methods for the haemolysis of human erythrocytes. (1957) (6)
Hb Doha or alpha 2 beta 2[X-N-Met-1(NA1)Val----Glu]; a new beta-chain abnormal hemoglobin observed in a Qatari female. (1985) (6)
Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantities. (1990) (6)
HB Porto Alegre or α2β29(A6) SER→CYS in Unrelated Families of the Canary Islands (1993) (6)
HEMOGLOBIN‐Q‐INDIA (64 (E13) ASP‐HIS) AND BETA THALASSEMIA: A CASE REPORT FROM PUNJAB (NORTH INDIA): To the Editor: (1988) (6)
The Occurrence and Identification of α-Thalassemia-2 among Hemoglobin S Heterozygotes (1981) (6)
A mild type of Hb S-beta(+)-thalassemia [-92(C-->T)] in a Sicilian family. (1993) (6)
Possible relationship between the level of Hb Bart's (gamma4) and the relative amount of Hb S or Hb C in black heterozygous newborn. (1978) (6)
HB Shelby [α2β2131(H9)GLN→LYS]-β°-Thalassemia [Codon 15 (TGG→TGA)] Identified by DNA Sequencing (1992) (6)
Further evidence for non-linkage of the Hb and Hb structural loci in man. (1972) (6)
Hb Lepore-Baltimore in a north Sardinian family. (1990) (6)
Hb ananosa or α2111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α2123(H6)Ala → Serβ2 (αl Mutation) are two silent stable variants detected by sequencing of amplified dna (1995) (6)
Hb Volga or α2β227(B9)Ala→Asp in an Italian Family (1985) (6)
Hemoglobin Babinga or alpha 2 delta 2 136 Gly--Asp observed in the American Negro. (1969) (6)
HB F-Sacromonte or α2Gγ259(E3)LYS→GLN Observed in a Spanish Newborn and His Mother (1993) (6)
Hb E-Saskatoon or α2β222(B4)Glu→Lys in a Spanish Family (1987) (6)
Hb Beograd (α2β2 121 (GH4) Glu → Val) Observed In A New Yugoslavian Family (1978) (6)
Two different quadruplicated alpha globin gene arrangements. (1987) (6)
Alpha-, beta-, and gamma-mRNA levels in beta-thalassemia; transcriptional and translational differences in heterozygotes, homozygotes, and compound heterozygotes. (1997) (6)
Hb-J-Georgia = Hb-J-Baltimore = α2β216Gly → Asp (1971) (6)
Hb F-Columbus-Ga or a2 Gγ2 94(FGJ)Asp→Asn (1982) (6)
The GγT Chain (Gγ75 Thr; 136 Gly) In Hb F-Charlotte Is The Product Of An Aγ Gene With A Limited Gene Conversion And That In Hb F-Waynesboro Of A Mutated Gγ Gene (2009) (6)
Hb Grady and alpha thalassemia: a contribution to the problem of the number of Hb alpha structural loci in man. (1976) (6)
HB Chandigarh or α2β294(FGl)ASP→GLY Observed in an Indian Family (1989) (6)
Hemoglobin Queens (α 34 (B15) Leu Arg) Found in two Chinese Families (1982) (6)
Hb A2-Zagreb Or α2δ2125(H3)Gln→Lglu, A New δ Chain Variant in Association with δβ-Thalassemia (1983) (6)
First observation of hemoglobin J Paris I [alpha-2-12(A10)alanine-aspartic acid beta-2] in the Indian subcontinent. (1988) (6)
Molecular characterization of beta-thalassemia in Azerbaijan. (1992) (6)
Two independent genetic factors in the beta-globin gene cluster are associated with high G gamma-levels in the HbF of SS patients. (1984) (5)
Hemoglobin G-San Jose (α2β27(A4)Glu←gly) in a Mexican Family (1980) (5)
Hb S-Hb Lufkin disease in a black male infant. (1995) (5)
Alpha-Thalassemia and fetal hemoglobin [letter] (1994) (5)
Hb F-Dammam or α2AΓ279(Ef3)Asp→Asn (1985) (5)
Hb Sabine or alpha 2 beta 2 91 (F7) Leu----Pro in a Yugoslavian boy. (1983) (5)
Some observations about the heterogeneity of haemoglobin in aluminum oxide chromatography. (1956) (5)
Abnormal human haemoglobins in western Kenya. (1984) (5)
Homozygotes for the hereditary persistence of fetal hemoglobin: The ratio of Gγ to Aγ chains and biosynthetic studies (1977) (5)
Hb Westmead [α122(H5)HIS→GLN], Hb E [β26(B8)6Ll→LYS], and α-Thamssemia-2 (3.7 KB Deletion) in a Laotian Family (1991) (5)
Hb Savaria or alpha2 (49)(CE7)Ser----Arg beta2 in an indigenous female from Kenya. (1985) (5)
Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family. (1991) (5)
Anomaly in the gamma chain heterogeneity of the newborn. (1977) (5)
The Frequency of the AγT Gene in the Presence and Absence of the βs or βC Gene in the Black Poplilation of the Southeastern USA (1981) (5)
First observation of haemoglobin Malay alpha 2B2 26 (B1) Asn----Ser--a case report. (1989) (5)
Analysis of high fetal hemoglobin production in sickle cell anemia patients from the Eastern Province of Saudi Arabia. (1987) (5)
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrow. (1995) (5)
A comparison of two procedures useful for the isolation of Hb F from adult red blood cells and for the quantitation of the types of gamma chain by high-performance liquid chromatography. (1984) (5)
Genetic heterogeneity of beta-thalassemia in southeast Sicily. (1995) (5)
Studies of the proporation and synthesis of haemoblogin C Philadelphia in red cells of heterozygotes, a homozygote, and a heterozygote for both haemoglobin G and alpha thalassaemia. (1976) (5)
The Effect of α-Thalassemia on the Level of Hybrid Hemoglobin Variants in Heterozygotes (1986) (5)
Types of α-globin gene deficiencies in chinese newborn babies in the Guangxi region, P. R. China (1992) (5)
The linkage of Hb Valletta [α2β287(F3)Thr→Pro] and Hb F-Malta-I [α2Gγ2117(G19)His→Arg] in the Maltese population (1991) (5)
Hb Cordele alpha(2)47 (CE5)Asp----Ala beta 2. A mildly unstable variant observed in black twins. (2009) (5)
Hb E and alpha-thalassemia; variability in the assembly of beta E chain containing tetramers. (1997) (5)
Two Rare Hemoglobin Variants: Hb Pyrgos [β83(ef7)Gly->Asp] and Hb Legnano [α141(hc3)arg->leu] Found in Inner Mongolia, P.R. China (1994) (5)
Search for nonallelic structural genes for γ-chains of fetal hemoglobin in some primates (1973) (5)
Synthesis of Hemoglobin chains in Adult and Newborn Goats: Possible Influence of the βc Synthesis on the Production of α CHAINS (1982) (5)
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia. (1989) (5)
The Mγ chain of human fetal hemoglobin; its identification and occurrence (1987) (5)
Clinical and Hematological Evaluation of two δ0 δ0 - Thalassemia Homozygotes (1981) (5)
Alpha-Thalassemia and fetal hemoglobin. (1994) (5)
HB N-Baltimore [α2β295(FG2)Lys→GLU] and HB J-Iran [α2β277(EF1]HIS→ASP] Observed in a Turkish Family from Antalya (1990) (5)
Hb Chad or α223(B4)GLU→LYSβ2 Observed in Members of a Surinam Family in Association with α-Thalassemia-2 and with HB S (1989) (5)
III. 3 – THE CYSTINE/CYSTEINE CONTENT OF HEMOGLOBINS (1959) (5)
HB Beth Israel (beta 102 [G4] Asn replaced by Ser) observed in a Yugoslavian teenager. (1978) (4)
The occurrence and identification of alpha-thalassemia-2 among hemoglobin S heterozygotes. (1981) (4)
The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants. (1996) (4)
Sheep hemoglobin D, an alpha-chain variant with one apparent amino acid substutution (alpha 15 Gly--Asp). (1968) (4)
HB A2-Liangcheng [δ117(G19)ASN→ASP(BC→GAC)]: A New δ Chain Variant Detected by Gene Analysis in a Chinese Family (1993) (4)
The Atlanta family with hemoglobin Grady revisited. (1983) (4)
Amino-acid composition of four different kinds of human haemoglobin. (1955) (4)
Hb G-Szuhu or α2β280(EF4)Asn→Lys, in Combination with β°-Thalassemia in a Spanish Family (1985) (4)
Myoglobins from Sheep Homozygous for Different Hæmoglobin Types (1957) (4)
Compound Heterozygosity for a Mild β+ and a Rare β°-Thalassemia Allele (1990) (4)
Hb Regina or alpha 2 beta 2 96(FG3)Leu----Val: a high oxygen affinity variant discovered by cation-exchange HPLC. (1985) (4)
Hb Davenport or alpha 2(78)(EF7)Asn----His beta 2. (1990) (4)
Homozygosity for a new type of G gamma (A gamma delta beta)zero-thalassemia in a Malaysian male. (1986) (4)
Hb Fort Worth Or α227 (B8)Glu→Glyβ2 in a Black Family from Canada (1985) (4)
The human fetal hemoglobins. (1980) (4)
Identification of the α chain abnormal hemoglobin Jackson (α127 Lys→Asn) after isolation of the core peptide by high-performance liquid chromatography (1983) (4)
A note on the inheritance of the hereditary persistence of fetal haemoglobin and the delta-chain variant Hb-A2'. (1976) (4)
Hemoglobin Montgomery (α2 48 Leu Arg β2) in a Chinese Family (1982) (4)
Usefulness of HPLC methodology for the characterization of combinations of the common beta chain variants Hbs S, C, and O-Arab, and the alpha chain variant Hb G-Philadelphia. (1993) (4)
Peripheral haemolysis, lipid peroxidation, iron status, and vitamin E in haemoglobin H syndromes in West Malaysia. (1993) (4)
Hb Zengcg or α2β2114(G16)Leu → Met (1990) (4)
Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations. (1992) (4)
Chromatography of Hemoglobin Variants (1974) (4)
Alpha and beta thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization. (1994) (4)
Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from Tunisia. (1992) (4)
Gene structure in hereditary persistence of fetal hemoglobin individuals. (1980) (4)
Two δ-Chain Abnormal Hemoglobins in One Individual. (1965) (4)
Annotation: HB Leslie is the Same as HB Shelby or α2β2131 (H9)GLN→LYS (1984) (4)
Relative Levels of α-, β-, and γ-mRNA from Patients with Severe and Intermediate β-Thalassemia Major (1997) (4)
Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatography. (1993) (4)
Hemoglobin F levels in patients with chronic renal failure. (1977) (4)
(A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA. (1985) (4)
A new Variant, Hb Muscat [α2β232(B14)Leu→val] Observed in Association With Hb S in an Arabian Family (1992) (4)
Hb A2-Wrens or alpha 2 delta 2 98(FG5) Val----Met, an unstable delta chain variant identified by sequence analysis of amplified DNA. (1989) (4)
HB F-Baskent or α2Aγ128 (H6)ALA→THR (1988) (4)
Characterization of three types of beta zero-thalassemia resulting from a partial deletion of the beta-globin gene. (1989) (4)
International Hemoglobin Information Center Variant List. (1994) (4)
HB Gainesville-GA or α2β246(CD5) Gly-Arg (1985) (4)
Hb Lepore-Baltimore (delta 68Leu-beta 84Thr) and Hb Lepore-Washington-Boston (delta 87Gln-beta IVS-II-8) in central Portugal and Spanish Alta Extremadura. (1997) (4)
Fetal hemoglobin heterogeneity in Chinese newborns of the Uygur and Han nationalities; comparisons of babies from Xinjiang and Beijing. (1987) (4)
Hb F-Bonaire-Ga or αAγ239(C5) Gln→Arg, Characterized by High Pressure Liquid Chromatographic and Microsequencing Procedures (1982) (4)
Organization of α-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, β-thalassemia, and α-thalassemia-2 (1982) (4)
Hemoglobin O-Padova or α230(B11)GLU→LYSβ2 observed in members of a Turkish family (1985) (4)
Hemoglobin Hofu or alpha 2 beta 2 [126 (H4) Va1 leads to Glu] found in combination with hemoglobin S. (1978) (4)
Identification and quantitation of hb olympia [β2O(b2)val → met] and hb san diego [β109(g11)val → met] by high-performance liquid chromatography (1983) (4)
Hemoglobin abnormalities in a black family with HB S, hereditary persistence of HB F, and a gamma chain variant; a reevaluation through gene mapping. (1984) (4)
Thalassemia intermedia in two patients with Hb lepore-β°-thalassemia (Frameshift codon 8, -AA) (1994) (4)
Hemoglobin D-β° Thalassemia A Case Report and Family Study (1988) (4)
Oxygen equilibrium analyses of isolated hemoglobins A2, Lepore-Washington and P-nilotic. (1978) (4)
Hb Brockton [alpha 2 beta 2(138)(H16)Ala-->Pro] observed in a Spanish girl. (1992) (4)
Polymorphic pattern of the (AT)X(T)Y motif at -530 5' to the beta-globin gene in over 40 patients homozygous for various beta-thalassemia mutations. (1994) (3)
The importance of the 3' untranslated region for the expression of the alpha-globin genes. (1996) (3)
HB f-xin-su or aγt73(e17)asp→his: A new slow-moving fetal hemoglobin variant (1987) (3)
Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family. (1991) (3)
α-Thalassemia and the production of different α chain variants in heterozygotes (1981) (3)
Chromatographic Behaviour of Hæmoglobin E (1956) (3)
Hb Gainesville-Ga or α2β246(Cd5) Gly→Arg; Second Report (1989) (3)
Persistent iron and folate deficiency in a patient with deletional hereditary persistence of fetal hemoglobin; the effect on the relative levels of Hb F and G gamma chains and the corresponding mRNAs. (1998) (3)
The polymorphism of human fetal hemoglobin. (1982) (3)
Hb F-Calluna or alpha 2 gamma 2(12 Thr replaced by Arg; 75Ile; 136Ala) in a Caucasian baby. (1983) (3)
Hb E-Saskatoon or alpha 2 beta 2(22)(B4)Glu----Lys in a Spanish family. (1987) (3)
Hb J-Pontoise or alpha 2(63)(E12)Ala----Asp beta 2 in four members of a Spanish family. (1987) (3)
Biosynthetic and structural studies of hemoglobin in a patient with congenital dyserythropoietic anemia type I. (1977) (3)
The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatography. (1984) (3)
Hemoglobin G Georgia or alpha 2-95 Leu (G-2) beta-2. (1970) (3)
A de novo deletion causing epsilon gamma delta beta-thalassemia in a Dutch patient. (1996) (3)
Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene. (1989) (3)
Hb F-Oakd or α2gγi226(B8)Glu → Lys (1987) (3)
Thalassemia in Southern India Interaction of Genes for β+-, β°-, and δ° β°-ThaIassemia (1980) (3)
Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family. (1989) (3)
Genetic aspects of gamma chain synthesis. (1972) (3)
The effect of pH on the uptake of methylene blue by human red cells. (1970) (3)
HB ottawa [alpha 15 (A13) GLY----ARG] found in Hubei Province, People's Republic of China. (1986) (3)
Hemoglobin Hamadan or alpha 2 beta 256(D7)Gly----Arg in a Turkish family. (1984) (3)
[Study on concentration of various amino acids in the cerebrospinal fluid]. (1955) (3)
Unstable Hb Newcastle [beta92(F8)His-->Pro], first case discovered in a Russian patient. (1999) (3)
Excretion of aminoacids in vitamin deficiency. (1954) (3)
HB F-Pendergrass, AH AΓI Variant with a Pro→Arg Substitution at Position Γ36(C2) (1985) (3)
Hb N-Baltimore [alpha 2 beta 2(95)(FG2)Lys----Glu] and Hb J-Iran [alpha 2 beta 2(77)(Ef1]His----Asp] observed in a Turkish family from Antalya. (1990) (3)
Structural characterization of two delta chain variants. Hemoglobin A'-2 (B2) and hemoglobin Flatbush. (1967) (3)
Chromatographic methods for the separation of normal and abnormal hemoglobins. (1980) (3)
HB F-Saskatoon or α2Gγ221(B3)GLU→LYS Observed in a North American Indian Newborn (1993) (3)
Hb Rainier or α2β2 (145(HC2)Tyr → Cys) Observed in Members of a Canadian Family of Greek Origin (1979) (3)
The structure of goat hemoglobins. V. A fourth beta chain variant (beta-D-Malta; 69 Asp is replaced by Gly) with decreased oxygen affinity and occurring at a high frequency in Malta. (1979) (3)
Alpha-thalassemia and the production of different alpha chain variants in heterozygotes. (1981) (3)
HB Mizuho or alpha 2 beta 2 68(E12)Leu-->Pro in a young Dutch boy. (1995) (3)
Hb Lulu Island (alpha 2 beta 2 107[G9]Gly-->Asp)-beta zero- thalassemia (codon 15; TGG-->TAG), a form of thalassemia intermedia. (1995) (3)
HB Köln or α2β298(FG5)VAL→MET in a Czechoslovakian Family (1991) (3)
DNA polymorphisms in north Sardinian newborns and their linkage with abnormal γ globin gene arrangements and with βo-thalassemia (1986) (3)
Hb Saint Louis or alpha 2 beta 2(28)(B10)Leu----Gln in a Czechoslovakian male. (1986) (3)
Long survival in sickle cell anemia. (1975) (3)
Two new large deletions resulting in epsilon gamma delta beta-thalassemia. (1988) (3)
The chemical heterogeneity of human hemoglobin F. Direct evidence for the existence of three types of gamma chain, the G gamma I, A gamma I, and A gamma T chains. (1979) (3)
The Importance of the 3′ Untranslated Region for the Expression of the α-Globin Genes (1996) (3)
Hb Winnipeg or α2, 75(Ef4)Asp→Tyrβ2 in a Large Caucasian Family Living in Georgia, Usa (1983) (3)
A mutation associated with elevated G gamma chain in sickle cell anemia and hereditary persistence of fetal hemoglobin. (1985) (3)
The use of globin chain electrophoresis in polyacrylamide gels for the quantitation of the G gamma to A gamma ratio in fetal hemoglobin. (1981) (3)
Different zeta globin gene deletions among black Americans. (1986) (3)
The Mγ chain of human fetal hemoglobin is an Aγ chain with an in vitro modification of γ141 leucine to hydroxyleucine (1993) (3)
Hb Mizuho or alpha 2 beta (2)68(E12)Leu----Pro in a Caucasian boy with high levels of Hb F; identification by sequencing of amplified DNA. (1991) (3)
Hb Etobicoke, alpha 85(F5) Ser leads to Arg found in a newborn of French-Indian-English descent. (1983) (3)
Hemoglobin Riyadh-β°-Thalassemia in an Indian Family (1979) (3)
δβ ‐Thalassaemia in Two Yugoslavian Families (2009) (3)
The relative levels of different types of beta-mRNA and beta-globin in BFU-E derived colonies from patients with beta chain variants; further evidence for somatic mosaicism in the Hb Costa Rica carrier [beta 77(EF1)His-->Arg]. (1996) (3)
The vγ chain of fetal hemoglobin of the orangutan (1978) (3)
Hb Albany-GA or a 2 11(A9)Lys?Asn 2 (1983) (3)
Introduction: Policies of The International Hemoglobin Information Center (1991) (3)
Black α-Thalassemia-1: Partial Characterization of an ∼80 KB Deletion Which Includes the ξ- and α-Globin Genes (1993) (3)
Homozygosity for hemoglobin O-Arab (alpha 2 beta 2 121 Glu----Lys). Hb O-Arab disease. (1986) (3)
Hb d-Granada or α2β222(b4)GLU→VAL (1987) (3)
Hb Bushwick [beta 74(E18)Gly----Val] heterozygotes in a Yugoslavian family have 35 to 40% of the unstable variant. (1987) (3)
On the quaternary structure of hemoglobin A-Ic. (1969) (3)
Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin gene. (1991) (3)
Simple Electrophoretic System for Presumptive Identification of Abnorm al Hemoglobins (3)
The Use of HPLC Procedures in the Study of Human Hemoglobin Variants (1985) (3)
Synthesis of a fixed-length single-stranded DNA probe by blocking primer extension in bacteriophage M13. (1986) (3)
Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia. (1989) (3)
Homozygotes for the hereditary persistence of fetal hemoglobin: the ratio of G gamma to A gamma chains and biosynthetic studies. (1977) (2)
Historical note: the beta-thalassemia allele in the noble Russian family Lermontov is identified as the ATG-->ACG change in the initiation codon. (1998) (2)
Types of alpha-globin gene deficiencies in Chinese newborn babies in the Guangxi region, P. R. China. (1992) (2)
Variation in clinical severity among patients with Hb Lepore-Boston-beta-thalassaemia is related to the type of beta-thalassaemia. (1988) (2)
A new beta zero-thalassaemia nonsense mutation (codon 112, T-->A) not associated with a dominant type of thalassaemia in the heterozygote. (1993) (2)
Oxygen equilibrium of haemoglobin A2 and its variant haemoglobin A2-1 (or B2). (1962) (2)
An elongated segment of DNA observed between two human α globin genes (1986) (2)
Hb Madrid or alpha 2 beta (2)115(G17)Ala-->Pro in a black teenager. (1993) (2)
Recombinant hemoglobin variants. (1998) (2)
Hb Winnipeg or alpha 2 75(EF4)Asp leads to Tyr beta 2 in a large Caucasian family living in Georgia, USA. (1983) (2)
Studies on bovine transferrin; isolation and partial characterization (2009) (2)
gamma-mRNA and Hb F levels in beta-thalassaemia. (1994) (2)
Differences between the levels of Gγ chain in the fetal hemoglobin in two types of hereditary persistence of fetal hemoglobin are linked with a variation in the DNA sequence (1986) (2)
I. Alteration in the properties of human hemoglobin A by variation in structure: a correlation of structure and function. (1970) (2)
HB A2−Grovetown or α2δ275(El9)Leu→val (1993) (2)
Separation of tryptic peptides of normal and abnormal alpha, beta, gamma, and delta hemoglobin chains by high-performance liquid chromatography. (1979) (2)
THE APPLICATION OF THE AGAR-GEL ELECTROPHORESIS ACCORDING TO WIEME TO THE IDENTIFICATION OF HEMOGLOBIN TYPES. (1963) (2)
gamma-Globin gene triplication and quadruplication in Japanese newborns. Evidence for a decreased in vivo expression of the 3'-A gamma-globin gene. (1985) (2)
A G to A nucleotide substitution 161 base pairs 5' of the G gamma globin gene cap site (-161) in a high G gamma non-anemic person. (1987) (2)
Globin Gene Regulation (1995) (2)
A newly discovered beta O-thalassemia (IVS-II-850, G-->A) mutation in a north European family. (1995) (2)
An Individual with Hb-Lepore-Baltimore- δβ-Thalassaemia in a Yugoslavian Family (2009) (2)
The amino acid sequence of the delta-beta chains of hemoglobin Lepore Augusta = Lepore Washington. (1966) (2)
Interaction Between Human Hemoglobin Variants and Hemoglobin S (1978) (2)
Hb Fukuyama or alpha 2 beta(2)77(EF1)His----Tyr observed in an Indonesian female. (1991) (2)
Hb Himeji or alpha 2 beta 2(140)(H18)Ala----Asp in a Portuguese family. (1989) (2)
Hb Coimbra or alpha 2 beta (2)99(G1)Asp----Glu, a newly discovered highoxygen affinity variant. (1991) (2)
The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA. (1992) (2)
Hb F-Brooklyn or α2Gγ266(E10)LYSGLN (1990) (2)
Hemoglobin Handsworth or alpha2 18(A16)Gly----Arg beta2 in a Saudi newborn. (1985) (2)
Posttranslational modification of beta 141 Leu associated with the beta 75(E19)Leu-->Pro mutation in Hb Atlanta. (1993) (2)
Hb J-Lome or α2β259(E3) Lys→Asn in a Vietnamese family (1989) (2)
Hemoglobin S-Ga Georgia disease: a case report. (1974) (2)
Nucleotide Sequence of the Human 01-Globin Gene (1988) (2)
Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure. (1988) (2)
Hemoglobin H disease in two Turkish females and one Iranian newborn. (1985) (2)
Hb F-Cle or α2gγ265(E9)Lys → Asn (1987) (2)
The Structure of Goat Hemoglobins (2003) (2)
Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140. (1988) (2)
Detection of the alpha-thalassemia-2 (3.7 kb) deletion in DNA extracted from 20-year-old blood smears. (1997) (2)
Hb F-Beech Island or alpha 2A gamma 2(53)(D4)Ala----Asp. (1985) (2)
Separation and Characterization of Hemoglobins (1976) (2)
Hb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencing. (1992) (2)
Hb Brockton [alpha 2 beta 2138(H16)Ala----Pro] observed in a Turkish girl. (1989) (2)
Identical nucleotide sequences of the 3'A gamma globin gene enhancer elements from four different chromosomes. (1989) (2)
A new gamma chain variant: Hb F-Pordenone [gamma 6(A3) Glu replaced by Gln: 75ILE: 136ALA]. (1982) (2)
Hemoglobin D-beta (0) thalassemia. A case report and family study. (1988) (2)
An Indonesian family with the Southeast Asian type of alpha-thalassemia-1 and a gamma-globin gene triplication. (1987) (2)
Is the trimodality of Hb Leslie (alpha 2 beta 2 131 Gln---O) in heterozygotes the result of a variable number of active alpha-chain genes? Evidence for posttranslational control of hemoglobin synthesis. (1978) (2)
An individual with “Miyada”-like hemoglobin indistinguishable from hemoglobin A2 (1973) (2)
Hb J-Lome or alpha 2 beta 259(E3)Lys----Asn in a Vietnamese family. (1989) (2)
Hb Ramona or α224(B5)TYR->CYSβ2 (1994) (2)
Evidence of a second foetal haemoglobin in the newborn goat. (1957) (2)
Nucleotide sequence of the humanθ1-globin gene (1988) (2)
HB F-Meinohama or α2γ2 (5 GLU-GLY; 75 ILE; 136 GLY) (1981) (2)
Hemoglobin-Strumica or alpha 2 112(G19) His replaced by Arg beta 2. (With an addendum: hemoglobin-J-Paris-I, alpha 2 12(A10) Ala replaced by Asp beta 2, in the same population). (1975) (2)
Heterozygosity and homozygosity for the high oxygen affinity hemoglobin Tarrant or alpha 126 (H9) Asp replaced by Asn in two Mexican families. (1981) (2)
Policies of the International Hemoglobin Inforwition Center Laboratory of Protein Chemistry Department of Biochemistry and Molecular Biology Medical College of Georgia Augusta, GA 30912-2100, USA (1989) (2)
Three sickle cell anemia patients each with a different α chain variant. Diagnostic complications (1993) (2)
HB Chapel Hill or α274(EF3)Asp→Glyβ2 observed in a chinese family in association with β-thalassemia (2009) (2)
Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr. (1988) (2)
HB Camperdown or α2β2104(G6)Arg→ser in Two Italian Males (1990) (2)
Compound heterozygosity for a mild beta (+) and a rare beta(0)-thalassemia allele. (1990) (2)
A Second Observation of HB Abruzzo [α2β2143(H21)HIS→ARG] in an Italian Family (1990) (2)
Hemoglobin daneshgah-Tehran or α272(ef1)his→argβ2 in an argentinean family (1985) (2)
Hb Nunobiki or alpha 2 141 (HC3)Arg-->Cys beta 2 in a Belgian female results from a CGT-->TGT mutation in the alpha 2-globin gene. (1996) (2)
Hb Bicêtre or alpha 2 beta(2)63(E7)His----Pro in a white male: clinical observations over a period of 25 years. (1986) (2)
Hb Iowa or alpha 2 beta 2(119)(GH2)Gly----Ala. (1990) (2)
The thalassemia syndromes in association with hemoglobinopathies in southern China. (1988) (2)
Oxygen Equilibria of Red Cell Hæmolysates of Adult Individuals, Heterozygous for Different Rare Abnormal Hæmoglobins (1964) (2)
Biochemical and molecular aspects of beta-thalassemia types in northern Sardinia. (1988) (2)
Hb F-Jiangsu, The First γ Chain Variant with a Valine -Methionine Substitution: αγ2134(H12) Val→Met (1990) (2)
Identification of the alpha chain abnormal hemoglobin Jackson (alpha 127 Lys leads to Asn) after isolation of the core peptide by high-performance liquid chromatography. (1983) (2)
HB F-Cobb OR α2Aγ237(C3)TRP→GLY (1985) (2)
Hb Cleveland or alpha 2 beta 2(93)(F9)Cys----Arg;121(GH4)Glu----Gln. (1991) (2)
An unusual phenotypic expression of Hb-Leiden (1982) (2)
Detection of the embryonic zeta chain in blood from newborn babies by reversed-phase high-performance liquid chromatography. (1987) (2)
Two rare hemoglobin variants: Hb Pyrgos [beta 83(EF7)Gly-->Asp] and Hb Legnano [alpha 141(Hc3)Arg-->Leu] found in Inner Mongolia, P. R. China. (1994) (2)
The first homozygote for the hereditary persistence of fetal hemoglobin observed in the southeastern United States. (1981) (2)
Hb F-Onoda or α2Gγ2146(HC3)Histyr a Newly Discovered Fetal Hemoglobin Variant in a Japanese Newborn (1990) (2)
Crystallography and oriented single crystal electron microscopy of hemoglobin deer II, a hemoglobin that exhibits matchstick-shaped erythrocytes. (1978) (2)
HB Ethiopia or α2140(HC2)TYR→HISβ2 (1992) (2)
Hb P-Nilotic or alpha 2(beta delta)2 in a Turkish family. (1987) (2)
HB Chiapas α2 114 PRO+ARG β2: Identification by High Pressure Liquid Chromatography (1981) (2)
The M gamma chain of human fetal hemoglobin is an A gamma chain with an in vitro modification of gamma 141 leucine to hydroxyleucine. (1993) (2)
Detection and quantitation of the fetal hemoglobin variant Hb F-Malta-I in adults (1977) (2)
Low quantities of Hb Boyle Heights or alpha 2(6)(A4)Asp----O beta 2 observed in three members of a Caucasian family. (1990) (2)
The Role of a Sickle Cell Center in Comprehensive Screening and Counseling for Sickle Cell and Related Disorders (1974) (1)
The Excretion of Sugars After the Intravenous Administration of Invert Sugar (1953) (1)
Hb Summer Hill or α2β252(D3)Asp→His in a Turkish Family from Cyprus (1983) (1)
Sickle cell anemia identified in a multiple-transfused patient through analysis of mRNA with an RT-PCR-based technique. (1995) (1)
Nucleotide sequence of the human theta 1-globin gene. (1988) (1)
Thalassemia intermedia caused by heterozygosity for both beta-thalassemia and hemoglobin Saki [beta 14 (A11) Leu replaced by Pro]. (1976) (1)
Hb F-Marietta or G gamma I 80[EF4] Asp replaced by Asn, observed in a Caucasian baby. (1982) (1)
Misdiagnosis of Combinations of Hb S and Other β-Chain Abnormal Hemoglobins Using a Simple Electrophoretic Procedure (1981) (1)
Hemoglobin O-Padova or alpha(2)30(B11)Glu----Lys beta 2 observed in members of a Turkish family. (1985) (1)
A second observation of Hb Abruzzo [alpha 2 beta 2(143)(H21)His----Arg] in an Italian family. (1990) (1)
Hb Nottingham (alpha2beta2 (FG5) 98 val leads to gly) in a Caucasian male: clinical and biosynthetic studies. (1978) (1)
[Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence o (1993) (1)
Hb Chiapas alpha 2 114 Pro replaced by Arg beta 2: identification by high pressure liquid chromatography. (1981) (1)
Hb Savaria or alpha(2)49(CE7)Ser----Arg beta 2 in a Yugoslavian family. (1985) (1)
Five haplotypes in Black beta-thalassaemia heterozygotes: three are associated with high and two with low G gamma values in fetal haemoglobin. (1985) (1)
A second family with HB minneapolis-Laos or α2β2118(GH1)phetyr (1987) (1)
Relative levels of alpha-, beta-, and gamma-mRNA from patients with severe and intermediate beta-thalassemia major. (1997) (1)
A note on the dissociation of human foetal haemoglobin at low pH. (1961) (1)
Two different theta (theta) globin gene deletions observed among black newborn babies. (1988) (1)
Beta-thalassemia due to frameshifts at codons 5, 6, 8, and 8/9; hematological observations in heterozygotes. (1990) (1)
The beta-delta crossover leading to the beta delta hybrid gene of hemoglobin P-Nilotic is located within 54 base-pairs of the 5' end of exon 2 or between codons 31 and 50. (1987) (1)
Hb-Alberta or alpha2beta2 (101(G3) Glu replaced by Gly), a new high-oxygen-affinity hemoglobin variant causing erythrocytosis. (1976) (1)
9th Symposium Molecular Biology of Hematopoiesis (Part 4 of 12) (1995) (1)
The relative levels of beta A and beta S mRNAs in Hb S heterozygotes and in patients with Hb S-beta(+)-thalassaemia or Hb S-beta(+)-HPFH combinations. (1994) (1)
Hb Costa Rica or ·2‚277(EF1)His→Arg: the first example of a somatic cell mutation in a globin gene (1996) (1)
[Studies on hemoglobin abnormality in sickle cell anemia and sickle cell trait]. (1954) (1)
HB Sögn or α2β214(A11)LEU → ARG in Combination with an α-Thalassemia Heterozygosity (1996) (1)
Beta zero-thalassemia in association with a gamma-globin gene quadruplication. (1986) (1)
Beta-thalassemia repository. (1989) (1)
[Homozygote beta-thalassemia in 2 Dutch families]. (1989) (1)
The G gamma T chain (G gamma 75 Thr; 136 Gly) in Hb F-Charlotte is the product of an A gamma gene with a limited gene conversion and that in Hb F-Waynesboro of a mutated G gamma gene. (1995) (1)
Hb Extremadura or alpha 2 beta 2133 (H11)Val----Leu, a new mildly unstable hemoglobin in a Spanish female. (1989) (1)
Hb Rainier or alpha 2 beta 2 (145 (HC2) Tyr replaced by Cys) observed in members of a Canadian family of Greek origin. (1979) (1)
Hb A2-Manzanares or alpha 2 delta 2 121 (GH4) Glu replaced by Val, an unstable delta chain variant observed in a Spanish family. (1983) (1)
Hemoglobin Kariya or alpha 240(C5)Lys----Glu beta 2 in a Caucasian family from South Carolina. (1984) (1)
Hb Suresnes or alpha2 141(HC3) ArgyieldHis beta2 in a black family. (1978) (1)
Hb Ethiopia or alpha 2(140)(HC2)Tyr----His beta 2. (1992) (1)
HB F-Yamaguchi (gamma 75Thr, gamma 80Asn, gamma 136Ala) is associated with G gamma-thalassemia. (1984) (1)
The structure of sheep hemoglobins. 3. Structural studies on the alpha chain of hemoglobin A. (1968) (1)
A second patient with hemoglobin Alberta, a high-oxygen-affinity variant causing erythrocytosis and forming asymmetric tetramers. (1978) (1)
Hb F-Dammam or alpha 2A gamma 2(79) (EF3) Asp----Asn. (1985) (1)
A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G----A)] complicated by the presence of an alpha-globin gene triplication. (1991) (1)
Hb Beograd (alpha2 beta2 121 (GH4) Glu replaced by Val) observed in a new Yugoslavian family. (1978) (1)
Hb S, Hb G-Philadelphia and alpha-thalassemia-2 in a Black family. (1980) (1)
HB G-Copenhagen or alpha 2 beta 2(47) (CD6) Asp----Asn observed in a black newborn. (1985) (1)
Is alkali-resistant haemoglobin in cooley's anaemia different from foetal haemoglobin? (1956) (1)
Hb A2-Babinga, Hb S, and HPFH in members of a family from Creola, Alabama. (1984) (1)
The amino-acid composition of human adult and foetal carbonmonoxyhaemoglobin extimated by ion exchange chromatography. (1955) (1)
A new slow-moving hemoglobin variant Hb Tianshui or alpha 2 beta(2)39(C5)Gln----Arg, observed in a Chinese family living in Gansu. (1990) (1)
Molecular characterization of beta-thalassemia in north Jordan. (1994) (1)
The Levels of Abnormal Hemoglobin in Persons with Heterozygosities for an a Chain Variant and for β-Thalassemia (1997) (1)
Hb-J-Georgia=Hb-J-Baltimore= 2 2 16 Gly leads to Asp. (1971) (1)
The frequency of the gamma chain variant A gamma T in different populations, and its use in evaluating gamma gene expression in association with thalassemia. (1985) (1)
Hemoglobin Riyadh-beta 0-thalassemia in an Indian family. (1979) (1)
Two Rare α Chain Variants, Hb Dunn Or α26(A4)Asp→Asnβ2 and HB G-Pest or α274(EF3)ASP→ASNβ2 Observed in an indian and a Black Newborn (1983) (1)
Hb G-Taipei or beta 22(B4)Glu----Gly in a Chinese family living in The Netherlands. (1987) (1)
The Greek A gamma beta+-HPFH observed in a large black family. (1987) (1)
Hb Camperdown or alpha 2 beta 2(104)(G6)Arg----Ser in two Italian males. (1990) (1)
Fetal hemoglobin variants identified in adults through restriction endonuclease gene mapping methodology. (1985) (1)
Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family. (1985) (1)
Linkage of the , 8-Chain and 8-Chain Structural Genes of Human Hemoglobins (2007) (1)
Gene duplication of the alpha chain of goat hemoglobin: evidence from a homozygous mutant. (1968) (1)
alpha-Thalassemia and beta-thalassemia in a Turkish family. (1977) (1)
Beta-thalassemia intermedia in an Indian female with the Hb Hofu [beta 126(H4)Val-->Glu]-beta zero-thalassemia [codons 8/9 (+G)] combination. (1995) (1)
Two rare unstable beta chain variants, Hb Mozhaisk or alpha 2 beta 292(F8)His----Arg and Hb Djelfa or alpha 2 beta 298(Fg5)Val----Ala, each being observed for the second time. (1989) (1)
Hb Anamosa or alpha 2(111)(G18)Ala-->Val beta 2 (alpha 2 mutation) and Hb Mulhacen or alpha 2(123)(H6)Ala-->Ser beta 2 (alpha 1 mutation) are two silent, stable variants detected by sequencing of amplified DNA. (1995) (1)
The linkage of Hb Valletta [alpha 2 beta 287(f3)Thr----Pro] and Hb F-Malta-I [alpha 2G gamma 2117(G19)His----Arg] in the Maltese population. (1991) (1)
Heterogeneity of γ-globin chain synthesis in Saudi newborns (1991) (1)
Hb F-Charlotte, an A gamma variant with a threonine residue in position gamma 75 and a glycine residue in position gamma 136. (1990) (1)
Carboxymethyl-cellulose microchromatography for the quantitation of hemoglobin Bart's (gamma 4) and its use in the detection of the alpha-thalassemia conditions. (1980) (1)
Detection of a new hybrid alpha 2 globin gene among American blacks. (1988) (1)
Hemoglobin Russ or alpha-2-51-arg-beta-2. (1966) (1)
Subunit dissociation of the unstable hemoglobin Bibba (alpha 2-136Pro(H19)beta 2). (1970) (1)
The percentages of Hb F and of G gamma and A gamma chains in the Hb F synthesized by reticulocytes and BFUe-derived colonies of patients with sickle cell anemia. (1982) (1)
Hemoglobin Athens-Georgia, or alpha 2 beta 2 40(C6)Arg replaced by Lys, a hemoglobin variant with an increased oxygen affinity. (1976) (1)
A new gene deletion involving the alpha 2-, alpha 1-, and theta 1-globin genes in a black family with Hb H disease. (1992) (1)
Hemoglobin Hamilton or alpha 2 beta 2 11(A8)Val leads to Ile: a silent beta-chain variant detected by Triton X-100 acid-urea polyacrylamide gel electrophoresis. (1984) (1)
HB Strasbourg [β23(B5)VALASP]; a High Oxygen Affinity Variant Observed in a German Family (1998) (1)
A fetal hemoglobin with abnormal gamma-polypeptide chains: hemoglobin Warren. (1965) (1)
Delta Beta-Thalassaemia in two yugoslavian families. (1975) (1)
A Second Case of Bemoglobxn Grady, Repetitive in the Middle of the α Chain (1976) (1)
Differences in affinity of variant beta chains for alpha chains: a possible explanation for the variation in the percentages of beta chain variants in heterozygotes. (1977) (1)
Probable inclusion-body beta-thalassemia in a Chinese family. (1976) (1)
Hemoglobin-A2-Coburg or alpha2delta2116Arg leads to His (G18). (1975) (1)
Hb F-Vea or α2Gγ240(C6)Arg→Gly (1995) (1)
Identification of several alpha-globin gene variations in a small Laotian family. (1995) (0)
The in vivo expression of the globin genes of theβ cistron in γ-,δ-, andδβ-thalassemia heterozygotes (1994) (0)
Hb Graz or alpha 2 beta 2(2)(NA2)His-->Leu; a new beta chain variant observed in four families from southern Austria. (1992) (0)
Haemoglobin alpha chain duplication in Barbary sheep, Ammotragus lervia, Pallas, 1777. (1970) (0)
Haemoglobins D-Los Angeles (alpha2beta2 121 GLU leads to GLN) and J-Baltimore (alpha2beta2 16 GLY leads to ASP) in two Dutch families. (1975) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 2 of 12) (1995) (0)
HEMOGLOBIN RIYADH-B'-THALASSEMIA IN (1979) (0)
[Studies on excretion of amino acids under PAS administration]. (1954) (0)
Beta-thalassemia repository. (1990) (0)
Identity of the alpha-chains of the minor human haemoglobin components A2 and A2' with the alpha-chains of human haemoglobin A and F. (1961) (0)
International Hemoglobin Information Center variant list. (1996) (0)
[Determination of t-PA and PAI-1: recommendations for the collection of samples]. (1991) (0)
Hb Sassari or alpha (2)126(H9)Asp---His beta 2 observed in a family from Northern Sardinia. (1987) (0)
Hb F-Auckland [α2Gγ27 (A4)Asp→Asn] Observed in a Caucasian Newborn from Alabama (1985) (0)
Hb Borås or α2β288(F4)Leu → Arg in a South African Female (1987) (0)
Excretion of amino acids in normal children of different ages. (1957) (0)
Hb F-Pendergrass, an A gamma I variant with a Pro----Arg substitution at position gamma 36(C2). (1985) (0)
Clinical and hematological evaluation of two delta 0 beta 0-thalassemia homozygotes. (1981) (0)
Hb F-Columbus-Ga or alpha 2 G gamma 2 94(FGl) Asp replaced by Asn. (1982) (0)
Changes in the Nature of Human Fetal Hemoglobin During the First Year of Life (1970) (0)
Hemoglobin Savannah (B6(24) beta-glycine is greater than valine): an unstable variant causing anemia with inclusion bodies. (1971) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 12 of 12) (1995) (0)
Hb F-Tokyo or alpha 2G gamma 2 34(B16)Val----Ile, a silent gamma chain variant detected by reverse phase high performance liquid chromatography. (1985) (0)
Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb S. (1989) (0)
An s 300 bp deletion involving part of the 5' beta globin gene region is observed in members of a turkish family with beta thalassemia (1987) (0)
Thalassemias in China (1987) (0)
Hb F-Kennestone or alpha 2G gamma 2 (EF1)77 His leads to Arg observed in a Caucasian baby. (1983) (0)
Identification and quantitation of Hb Olympia [beta 20(B2)Val leads to Met] and Hb San Diego [beta 109(G11)Val leads to Met] by high-performance liquid chromatography. (1983) (0)
Hb J-Singa (alpha-78 Asn leads to Asp), a newly discovered hemoglobin variant with the same amino acid substitution as one of the two present in Hb J-Singapore (alpha-78 Asn leads to, alpha-79 Ala leads to Gly). (1984) (0)
Thalassemia in southern India. Interaction of genes for beta+-, beta o-, and delta o beta o-thalassemia. (1980) (0)
II. Binding of organic phosphates to hemoglobin. (1970) (0)
3. Hemoglobin heterogeneity and structural genes. (1970) (0)
Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn. (1987) (0)
Book Review:Sickle Cell Anemia and Other Hemoglobinopathies. Richard D. Levere (1976) (0)
Hemoglobin Chapel Hill or alpha2 74 Asp replaced by Gly beta2. (1976) (0)
Brief Reports of Rare Human Hemoglobin Variants (1983) (0)
Hb F-Auckland [alpha 2G gamma 2(7)(A4)Asp----Asn] observed in a Caucasian newborn from Alabama. (1985) (0)
Hb G-Szuhu or alpha 2 beta 2(80)(EF4)Asn----Lys, in combination with beta zero-thalassemia in a Spanish family. (1985) (0)
Hb Sögn or alpha 2 beta 2 14(A11)Leu-->Arg in combination with an alpha-thalassemia heterozygosity. (1996) (0)
The in vivo expression of the globin genes of the beta cistron in gamma-, delta-, and delta beta-thalassemia heterozygotes. (1994) (0)
Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama. (1995) (0)
Some physicochemical properties of hemoglobin-manitoba (alpha2 102Ser replaced by Arg (G9) beta2). (1975) (0)
Hemoglobin Atlanta or alpha 2 beta 2 75 Leu-Pro (E19): an unstable variant found in several members of a Caucasian family. (1975) (0)
The V gamma chain of fetal hemoglobin of the orangutan. (1978) (0)
Hb Olomouc or alpha 2 beta 2(86)(F2)Ala----Asp, a new high oxygen affinity variant. (1987) (0)
A second observation of Hb F-Lodz or alpha 2G gamma (2)44(CD3)Ser----Arg. (1991) (0)
The determination of the percentages of G gamma and A gamma chains in human fetal hemoglobin by HPLC. (1980) (0)
[Amino acid excretion of normal children of different ages]. (1957) (0)
Hb F-Cobb or alpha(2)A gamma(2)37(C3)Trp----Gly. (1985) (0)
Hb Nottingham or alpha 2 beta 2(98)(FG5)Val----Gly observed as a de novo mutation in a Canadian child. (1992) (0)
Hb F-Brooklyn or alpha 2G gamma 2(66)(E10)Lys----Gln. (1990) (0)
[Preferential synthesis of fetal hemoglobin in in vitro cultures of erythroid precursors from peripheral blood of healthy persons and those with hemoglobinopathies]. (1979) (0)
Hemoglobin Queens (alpha 34 (B15) Leu replaced by Arg) found in two Chinese families. (1982) (0)
To the Readers of the Journal Hemoglobin (1998) (0)
[Elimination of amino acids in normal children of various ages]. (1957) (0)
[The Giri method in qualitative paperchromatographic analysis of aminoacids in biological liquids]. (1955) (0)
A new delta chain variant, haemoglobin-A2-Melbourne or alpha2 delta2 43Glu-Lys(CD2). (1974) (0)
Amperometric titration of sulphydryl groups in human haemoglobin with silver nitrate. (1958) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 9 of 12) (1995) (0)
Investigations concerning the Abnormal Haemoglobin in Sicklaemia and Sickle-Cell Trait. (1954) (0)
Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family. (1988) (0)
Hb F-Saskatoon or alpha 2G gamma (2)21(B3)Glu-->Lys observed in a North American Indian newborn. (1993) (0)
P Thalassemia-Hemoglobin D a . A Family Report (2007) (0)
Hb F-Onoda or alpha 2G gamma 2(146)(HC3)His----Tyr, a newly discovered fetal hemoglobin variant in a Japanese newborn. (1990) (0)
IV. The chemical heterogeneity of the chain from human fetal hemoglobin. (1970) (0)
Hemoglobin Jenkins or hemoglobin-N-Baltimore or alpha-2-beta-2 95Glu. (1966) (0)
Hb Las Palmas or alpha 2 beta 2(49)(CD8)Ser----Phe, a mildly unstable hemoglobin variant. (1988) (0)
A new variant, HB Muscat [alpha 2 beta (2)32(B14)Leu----Val] observed in association with HB S in an Arabian family. (1992) (0)
Hb Strasbourg [beta 23(B5)Val-->Asp]; a high oxygen affinity variant observed in a German family. (1998) (0)
Hb Gainesville-GA or alpha 2 beta 2(46)(CD5)Gly----Arg; second report. (1989) (0)
An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease. (1971) (0)
Hmoglobin Alamo [α2 β2 19(BL) ASNàASP] (2009) (0)
Hb A2-liangcheng [delta 117(G19)Asn->Asp(AAC->GAC)]: a new delta chain variant detected by gene analysis in a Chinese family. (1993) (0)
Hb F-Xin-Su or A gamma I73(E17)Asp----His: a new slow-moving fetal hemoglobin variant. (1987) (0)
[Properties and determination methods of abnormal human hemoglobins]. (1959) (0)
Abnormal gamma-globin gene arrangements in Sardinians. (1988) (0)
Hb Ottawa [α15(A13) GLY→ARG] found in Hubei Province, People’s Republic of China (2008) (0)
Abnormal hemoglobins in Malta : the significance of two fetal and an adult variant (1972) (0)
Letter: Hereditary persistence of foetal haemoglobin. (1975) (0)
Hb Albany-GA or alpha 2(11)(A9)Lys leads to Asn beta 2. (1983) (0)
Hb Fort Worth or alpha2 27(B8)Glu----Gly beta2 in a black family from Canada. (1985) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 7 of 12) (1995) (0)
The ratio of G gamma and A gamma chains of the hemoglobin F synthesized by BFU-E-derived colonies from blood of subjects with beta+ thalassemia and related hemoglobinopathies. (1980) (0)
[Effects of a mixture of sodium citrate and citric acid in a case of severe rickets]. (1953) (0)
Hb F-Sacromonte or alpha 2G gamma (2)59(E3)Lys-->Gln observed in a Spanish newborn and his mother. (1993) (0)
The Ggamma deltabeta-thalassemia and Ggamma-betaO-hpfh conditions in combination with beta-thalassemia and Hb S. (1977) (0)
An X-ray determination of the molecular interactions in hemoglobin C: a disease characterized by intraerythrocytic crystals. (1979) (0)
Hb F-Jiangsu, the first gamma chain variant with a valine----methionine substitution: alpha 2A gamma 2 134(H12)Val----Met. (1990) (0)
[Case of chronic renal insufficiency with nephrocalcinosis]. (1954) (0)
Introduction of a New Feature Section Brief Reports of Rare Human Hemoglobin Variants (1983) (0)
Hb F-La Grange or alpha 2 gamma 2 101(G3)Glu----Lys; 75Ile; 136Gly: a high oxygen affinity fetal hemoglobin variant observed in a Caucasian newborn. (1984) (0)
Hb Vaasa or alpha2beta2 (39(C5)Gln replaced by Glu), a mildly unstable variant found in a Finnish family. (1977) (0)
Investigations into the secretion of amino acids in the urine of rachitic children. (1954) (0)
A novel beta zero-thalassaemia mutation (codon 15, TGG----TGA) is prevalent in a population of central Portugal. (1992) (0)
Hb F-Catalonia or alpha 2G gamma(2)15(A12)Trp----Arg. (1990) (0)
Abnormal Haemoglobins (1957) (0)
The frequency of the A gamma T gene in the presence and absence of the beta S or beta C gene in the Black population of the Southeastern USA. (1981) (0)
An elongated segment of DNA observed between two human alpha globin genes. (1986) (0)
[Hemoglobin Complutense (beta 127 (H5) Gln replaced by Glu) in a Spanish family]. (1987) (0)
Hemoglobin Fort Gordon or alpha2beta2145 Tyr replaced by Asp, a new high-oxygen-affinity hemoglobin variant. (1975) (0)
Hb A2-Zagreb or alpha 2 delta 2(125)(H3)Gln replaced by Glu, a new delta chain variant in association with delta beta-thalassemia. (1983) (0)
Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2. (1982) (0)
[Molecular characterization of a Spanish family with alpha-thalassemia]. (1988) (0)
The levels of abnormal hemoglobin in persons with heterozygosities for an alpha chain variant and for beta-thalassemia. (1997) (0)
Hb F-Kingston or alpha 2G gamma 2(55)(D6)Met----Arg in a Spanish newborn. (1987) (0)
[Structural variants in hemoglobin occurring in the Czech Republic]. (1995) (0)
[Hemoglobin F Catalonia. A new variant of fetal hemoglobin]. (1991) (0)
Hb-Genova ( 2 2 28(B10)Leu leads to Pro ); methods for detection and analysis of unstable hemoglobins. (1973) (0)
Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant. (1982) (0)
Three sickle cell anemia patients each with a different alpha chain variant. Diagnostic complications. (1993) (0)
Hb Costa Rica or alpha 2 beta 2 77(EF1)His --> Arg: the first example of a somatic cell mutation in a globin gene. (1996) (0)
Hb A2-Grovetown or alpha 2 delta (2)75(E19)Leu-->Val. (1993) (0)
Hb Gainesville-GA or alpha 2 beta 2 46(CD5)Gly----Arg. (1985) (0)
Hb Chandigarh or alpha 2 beta 2(94)(FG1)Asp----Gly observed in an Indian family. (1989) (0)
Hemoglobin Beograd or alpha 2 beta 2 121 Glu-Val (GH4). (1973) (0)
Two Families with Abnormal Haemoglobin C. (1955) (0)
Two rare alpha chain variants, Hb Dunn or alpha 26(A4)Asp replaced by Asn beta 2 and Hb G-Pest or alpha 274(EF3)Asp replaced by Asn beta 2, observed in an Indian and a black newborn. (1983) (0)
Zeta and theta 1-globin gene deletions located on the same chromosome. (1989) (0)
Synthesis of hemoglobin chains in adult and newborn goats: possible influence of the beta c synthesis on the production of alpha chains. (1982) (0)
Hb Ramona or alpha (2)24(B5)Tyr-->Cys beta 2. (1994) (0)
Hemoglobin G-San Jose (alpha 2 beta 2 7(A4)Glu replaced by Gly) in a Mexican family. (1980) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 5 of 12) (1995) (0)
The ratio of the G gamma and A gamma chains: variations due to anomalies at the molecular level. (1985) (0)
Heterogeneity of gamma-globin chain synthesis in Saudi newborns. (1991) (0)
Globin mRNA in beta-thalassemia heterozygotes with different beta-thalassemia alleles and in heterozygotes for hereditary persistence of fetal hemoglobin. (1996) (0)
Gamma-chain heterogeneity of fetal hemoglobin in nonblack beta- and delta beta- thalassemia and HPFH heterozygotes and homozygotes. (1982) (0)
Haplotypes and levels of fetal hemoglobin and G gamma to A gamma ratios in Mediterranean patients with thalassemia minor and major. (1985) (0)
Construction of three plasmids, each containing two or three different human globin gene fragments. (1988) (0)
The detection of hemoglobinopathies : [working papers] (1974) (0)
HB Oleander, α116(GH4)GLLàGLN, Found in a Black Female in Georgia (1984) (0)
Hb-Volga or alpha 2 beta 2 27(B9)Ala replaced by Asp. An unstable hemoglobin variant in three generations of a Dutch family. (1976) (0)
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes. (1990) (0)
Hb Leslie is the same as Hb Shelby or alpha 2 beta 2 131 (H9)Gln----Lys. (1984) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 11 of 12) (1995) (0)
Some observations on the estimation of single amino-acids in blood. (1953) (0)
Hb D-Granada or alpha 2 beta 2 22(B4)Glu----Val. (1987) (0)
Hb F-Oakland or alpha 2G gamma I2(26)(B8)Glu----Lys. (1987) (0)
Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identification. (1986) (0)
A Second Observation of HB F-Lodz or α2Gγ244(CD3)SER→ARG (1991) (0)
thalassemia and HPFH heterozygotes The gamma chain heterogeneity of fetal hemoglobin in black beta (2011) (0)
Four categories of gamma-globin gene triplications: DNA sequence comparison of low G gamma and high G gamma triplications. (1988) (0)
HB f-Kingston or α26γ255(d6)met→arg in a spanish newborn (1987) (0)
Structure of human hemoglobin C: a disease with intraerythrocytic crystals. (1979) (0)
Hb Zengcheng or alpha 2 beta(2)114(G16)Leu----Met. (1990) (0)
International Hemoglobin Information Center: policies--IHIC. (1982) (0)
50th Anniversary of Acta Haematologica (1998) (0)
Hemoglobin Alamo (alpha2beta2 19 (b1) Asn replaced by Asp). (1977) (0)
The properties, estimation methods, hematologic features, and some other more general aspects of different abnormal human hemoglobins. (1957) (0)
Hemoglobin A2-Indonesia or alpha 2 delta 2 69(E13) Gly--Arg. (1971) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 3 of 12) (1995) (0)
Characterization of abnormalities in the gamma-globin gene arrangements of Japanese newborns. (1988) (0)
A second family with Hb Minneapolis-Laos or alpha 2 beta (2)118(GH1)Phe----Tyr. (1987) (0)
Hb Köln or alpha 2 beta 2(98)(FG5)Val----Met in a Czechoslovakian family. (1991) (0)
The effect of glucose on the alloxan content of the blood. (1950) (0)
Application of high pressure liquid chromatography and microsequencing methodology in the structural analysis of human hemoglobin variants. (1983) (0)
Hb F-Meinohama or alpha 2 gamma 2 (5 Glu replaced by Gly; 75 Ile; 136 Gly). (1981) (0)
HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black family. (1986) (0)
An individual with Hb-Lepore-Baltimore- delta beta-thalassaemia in a Yugoslavian family. (1976) (0)
Chromatographic behavior of haemoglobin E. (1956) (0)
Search for nonallelic structural genes for gamma-chains of fetal hemoglobin in some primates. (1973) (0)
Subject Index Vol. 93,1995 (1995) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 8 of 12) (2004) (0)
Hb Borås or alpha 2 beta 2(88)(F4)Leu----Arg in a South African female. (1987) (0)
Hb F-Veleta or alpha 2 G gamma(2)40(C6)Arg-->Gly. (1995) (0)
[Excretion of free and combined amino acids during intravenous administration of protein hydrolysate]. (1954) (0)
Hb Guangzhou-Hangzhou or alpha 2(64)(E13)Asp----Gly beta 2 observed in members of a Chinese family living in Xinjiang. (1990) (0)
Thalassemia intermedia in two patients with Hb Lepore-beta zero-thalassemia (Frameshift codon 8, -AA). (1994) (0)
HB Guangzhou-Hangzhou or α264(E13)ASP→GLYβ2 Observed in Members of a Chinese Family Living in Xinjiang (1990) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 6 of 12) (1995) (0)
Hb Porto Alegre or alpha 2 beta 29(A6)Ser->Cys in unrelated families of the Canary Islands. (1993) (0)
Hb Volga or alpha 2 beta 2 27(B9)Ala----Asp in an Italian family. (1985) (0)
[Considerations on determination of various amino acids in blood]. (1953) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 10 of 12) (1995) (0)
The M gamma chain of human fetal hemoglobin; its identification and occurrence. (1987) (0)
[Studies on phenylalanine & tyrosine metabolism in scurvy in children]. (1957) (0)
The M gamma chain of human fetal hemoglobin. (1987) (0)
Construction of two plasmids, each containing three different human globin gene fragments. (1987) (0)
Viscosity and gelation studies in deer hunting hemoglobins. (1975) (0)
Hb Chapel Hill or alpha 274(EF3)Asp----Gly beta 2 observed in a Chinese family in association with beta-thalassemia. (1986) (0)
Hb Summer Hill or alpha 2 beta 2(52)(D3)Asp replaced by His in a Turkish family from Cyprus. (1983) (0)
[Observations in a case of glycogenosis]. (1954) (0)
DNA polymorphisms in North Sardinian newborns and their linkage with abnormal gamma globin gene arrangements and with beta (0) -thalassemia. (1986) (0)
Hemoglobin Hacettepe or alpha 2 beta 2 127 (H5) Gln replaced by Glu. (1976) (0)
β-Thalassemia repository (1990) (0)
9th Symposium Molecular Biology of Hematopoiesis (Part 1 of 12) (1995) (0)
Separation of the A gamma and G gamma cyanogen bromide peptides of human fetal hemoglobin by high-pressure liquid chromatography. (1979) (0)
Contents, Vol. 93, 1995 (1995) (0)
Hb F-Bonaire-Ga or alpha 2 A gamma 2 39(C5) Gln replaced by Arg, characterized by high pressure liquid chromatographic and microsequencing procedures. (1982) (0)
Hemoglobin-Bibba or alpha-2-136Pro-beta 2, an unstable alpha chain abnormal hemoglobin. (1968) (0)
Investigations on the abnormal haemoglobin in sicklaemia and sicklecell trait. (1955) (0)
[Haplotype in 3 patients homozygous for beta-thalassemia]. (1987) (0)
Hb Oleander, alpha 116(GH4)GLU----GLN, found in a Black female in Georgia. (1984) (0)
Policies of the International Hemoglobin Information Center (Ihic) Comprehensive Sickle Cell Center Medical College of Georgia Augusta, Ga 30912-1100, Usa (1987) (0)
The effect of alpha-thalassemia on the level of hybrid hemoglobin variants in heterozygotes. (1986) (0)
Myoblobins from sheep homozygous for different haemoglobin types. (1957) (0)
The amino acid composition of human adult, fetal and sickle cell carbonmonoxyhemoglobin. (1954) (0)
Hemoglobin F in beta thalassemia and related conditions. (1980) (0)
Amino-acid composition of adult and foetal myoglobin of the cow. (1957) (0)

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