Frederick Hecht

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Frederick Hecht is affiliated with the following schools: University of Washington, University of Rochester, Arizona State University, Harvard University, University of California, Berkeley, Dartmouth College, University of Oregon, Stanford University

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Frederick Hecht

Biology

#5606

World Rank

#8126

Historical Rank

#1909

USA Rank

Genetics

#513

World Rank

#588

Historical Rank

#200

USA Rank

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Biology

Frederick Hecht's Degrees

PhD Genetics University of California, Berkeley
Masters Biology Stanford University
Bachelors Biochemistry University of California, Berkeley

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Frederick Hecht's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Chromosome abnormalities and genetic counseling. (1990) (389)
Parthenogenic origin of benign ovarian teratomas. (1975) (359)
Somatic rearrangement of chromosome 14 in human lymphocytes. (1975) (266)
The journal "impact factor": a misnamed, misleading, misused measure. (1998) (215)
LEUKÆMIA AND LYMPHOCYTES IN ATAXIA-TELANGIECTASIA (1966) (203)
Congenital contractural arachnodactyly. A heritable disorder of connective tissue. (1971) (177)
Mutations of the Kirsten-ras proto-oncogene in human preleukaemia (1987) (154)
Fragile sites and cancer breakpoints. (1984) (151)
Common region on chromosome 14 in T-cell leukemia and lymphoma. (1984) (149)
Chromosome 14 translocation in african and north american burkitt's lymphoma (1977) (146)
Ring 22 chromosomes in dermatofibrosarcoma protuberans are low-level amplifiers of chromosome 17 and 22 sequences. (1995) (146)
Chromosome techniques. Theory and practice. (1973) (136)
Ataxia-telangiectasia--clonal growth of translocation lymphocytes. (1973) (133)
Heritable Fragile Site on Chromosome 16: Probable Localization of Haptoglobin Locus in Man (1970) (132)
Cancer in ataxia-telangiectasia patients. (1990) (129)
Chromosomes in kidney, ureter, and bladder cancer. (1986) (128)
SOCIAL CONTACTS AND LEUKÆMIA-LYMPHOMA: THE PHILADELPHIA CHROMOSOME REARRANGEMENT (1975) (123)
“Surely you're joking, Mr. Feynman!” Adventures of a curious character (1986) (119)
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME. (1964) (115)
Trisomy 13 (D1) syndrome: studies on parental age, sex ratio, and survival. (1968) (103)
"New" syndrome of congenital contractural arachnodactyly originally described by Marfan in 1896. (1972) (100)
Regional chromosome localization of human papillomavirus integration sites near fragile sites, oncogenes, and cancer chromosome breakpoints. (1988) (97)
Cancer chromosome breakpoints and common fragile sites induced by aphidicolin. (1984) (89)
Increased frequency of thyroid autoantibodies in mothers of patients with Down's syndrome. (1965) (85)
Abortion and the politics of motherhood. (1984) (84)
NUCLEAR ABNORMALITIES OF THE NEUTROPHILS IN D1 (13-15)-TRISOMY SYNDROME. (1964) (79)
Lysergic-acid-diethylamide and cannabis as possible teratogens in man. (1968) (79)
Human Embryonic Hæmoglobins (1964) (78)
13-cis retinoic acid treatment for myelodysplastic syndromes. (1986) (77)
Supernumerary ring chromosomes containing chromosome 17 sequences. A specific feature of dermatofibrosarcoma protuberans? (1994) (76)
HUMAN EMBRYONIC HEMOGLOBINS. (1964) (76)
Racial differences in the frequency of Q and C chromosomal heteromorphisms (1977) (72)
Fragile sites, cancer chromosome breakpoints, and oncogenes all cluster in light G bands. (1988) (71)
Common mechanism of chromosome inversion in B- and T-cell tumors: relevance to lymphoid development. (1986) (71)
Cytogenetic and immunophenotypic analysis of cell lines established from patients with T cell leukemia/lymphoma. (1986) (70)
Long-term growth of malignant thymocytes in vitro. (1989) (66)
THE NONRANDOMNESS OF CHROMOSOMAL ABNORMALITIES. ASSOCIATION OF TRISOMY 18 AND DOWN'S SYNDROME. (1964) (65)
Test-tube women. What future for motherhood? (1986) (65)
The No. 17–18 (E) trisomy syndrome (1963) (62)
Chromosome 5q35 breakpoint in malignant histiocytosis. (1986) (62)
REPRODUCTION AND MEIOSIS IN XYY (1967) (58)
Ring-G chromosome, a new G-deletion syndrome? (1968) (58)
Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia. (1981) (57)
Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome. (1970) (57)
Trisomy 4: an entity within acute nonlymphocytic leukemia. (1987) (57)
Clinical and biologic characterization of T-cell neoplasias with rearrangements of chromosome 7 band q34. (1988) (57)
Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation (1987) (55)
Familial predisposition to thyroid disease in Down's syndrome: controlled immunoclinical studies. (1971) (55)
Trisomy 13-15 in a male infant. (1962) (55)
Chromosome clues to acute leukemia in Down's syndrome. (1986) (53)
Genetic mechanisms of sexual development (1980) (53)
Chromosome 3 duplication q/deletion p syndrome. (1978) (53)
Origin of extragonadal teratomas and endodermal sinus tumours (1975) (51)
Impaired in vitro response of circulating lymphocytes to phytohemagglutinin in Down's syndrome: dose- and time-response curves and relation to cellular immunity. (1970) (51)
Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns (1984) (50)
Chromosomal abnormalities ascertained in the collaborative perinatal survey of 7- and 8-year-old children. (1979) (50)
Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis (1984) (49)
The Philadelphia chromosome: a model of cancer and molecular cytogenetics. (1986) (49)
Leukemia with Down's syndrome: translocation between chromosomes 1 and 19 in acute myelomonocytic leukemia following transient congenital myeloproliferative syndrome. (1985) (48)
New common fragile sites. (1988) (48)
Letter: Social contacts and leukaemia-lymphoma: the Philadelphia chromosome rearrangement. (1975) (48)
Predominance of Hemoglobin Gower 1 in Early Human Embryonic Development (1966) (47)
Nonrandomness of Translocations in Man: Preferential Entry of Chromosomes into 13-15/21 Translocaftons (1968) (47)
Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements. (1971) (46)
Philadelphia chromosome-positive acute lymphoblastic leukemia cell lines without classical breakpoint cluster region rearrangement. (1988) (46)
A guide to fragile sites on human chromosomes. (1990) (46)
Histiocytic lymphoma cell lines: immunologic and cytogenetic studies. (1985) (46)
Heritable dysmorphic syndrome with normal intelligence. (1967) (45)
Gregory bateson. The legacy of a scientist (1981) (45)
Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes. (1988) (45)
The fragile X syndrome. Diagnosis, biochemistry, and intervention. (1984) (44)
Acute myeloblastic leukemia (AML) with t(6;9) (p23;q34): a specific subgroup of AML? (1983) (44)
Winglets of the eye: dominant transmission of early adult pterygium of the conjunctiva. (1990) (43)
Fragile X-linked mental retardation. (1980) (43)
Construction of long-range restriction maps in human DNA using pulsed field gel electrophoresis. (1987) (41)
Mechanisms of giemsa banding of chromosomes. I. Giemsa-11 banding with azure and eosin. (1976) (40)
Responses of hemopoietic precursors to 13-cis retinoic acid and 1,25 dihydroxyvitamin D3 in the myelodysplastic syndromes. (1986) (40)
Chromosomal localization of the human genes for lipocortin I and lipocortin II. (1988) (40)
Are balanced translocations really balanced? Preliminary cytogenetic evidence for position effect in man. (1978) (39)
Deletion of chromosome band 13q14: a primary event in preleukemia and leukemia. (1985) (38)
Chromosomes in gliomatosis cerebri (1995) (37)
Double aneuploidy: the frequency of XXY in males with Down's syndrome. (1969) (36)
Annotation: genetic effects of aneuploidy. (1973) (36)
Three additional cases of the congenital hypothalamic "hamartoblastoma" (Pallister-Hall) syndrome. (1989) (35)
Direct prenatal chromosome diagnosis of a malignancy. (1984) (34)
Chromosome localization of human ARH genes, a ras-related gene family. (1990) (34)
The Philadelphia (Ph) chromosome in leukemia. II. Variant Ph translocations in acute lymphoblastic leukemia. (1985) (34)
Human and mammalian cytogenetics. An historical perspective (1980) (34)
Estimating distances from the centromere by means of benign ovarian teratomas in man (1976) (34)
Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-). (1972) (34)
The fragile X chromosome: current methods. (1982) (34)
Genetic counseling: Psychological dimensions (1980) (33)
THE INHERITANCE AND DEVELOPMENT OF THE NAIL-PATELLA SYNDROME (1963) (33)
Translocation (1;7)(p11;p11): a new myeloproliferative hematologic entity. (1985) (33)
A rearranged transforming gene, tre, is made up of human sequences derived from chromosome regions 5q, 17q and 18q. (1988) (32)
Chromosome subband 17p11.2 deletion: a minute deletion syndrome. (1988) (32)
XXY cells in a predominantly XX human male: evidence for cell selection. (1966) (31)
Translocations involving chromosomes #3 and #12: hematologic diseases associated with abnormalities of these chromosomes. (1982) (31)
TRISOMY-18 SYNDROME DUE TO DE-NOVO TRANSLOCATION (1963) (31)
Fragile sites limited to lymphocytes: molecular recombination and malignancy. (1987) (31)
Cytogenetic analyses in 89 patients with secondary hematologic disorders--results of a cooperative study. (1987) (30)
Chromosome change in transitional cell carcinoma of ureter. (1986) (29)
Incontinentia pigmenti in Arizona Indians including transmission from mother to son inconsistent with the half chromatid mutation model (1982) (27)
Solid tumor breakpoint update. (1988) (27)
Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II. (1972) (27)
Trisomy 4 in hematologic disorders. (1987) (26)
Mosaicism in Turner's syndrome reflects the lethality of XO. (1969) (26)
Partial trisomy 15. (1972) (25)
The importance of being a fragile site. (1979) (25)
Chromosome rearrangements in dysplastic nevus syndrome predisposing to malignant melanoma. (1988) (25)
Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studies. (1978) (25)
Letters to the Editors:Detection of fragile sites on human chromosomes (1985) (24)
Translocations in T-cell leukemia in lymphoma. (1985) (24)
Newborn infants with Hb Portland 1, an indicator of α‐chain deficiency (1968) (24)
Heraclitean fire. Sketches from a life before nature. (1979) (24)
Congenital cutis laxa with retardation of growth and motor development: a recessive disorder of connective tissue with male lethality (1986) (24)
Hemoglobin-Seattle (α2Aβ276 Glu): An Unstable Hemoglobin Causing Chronic Hemolytic Anemia (1970) (23)
Aneuploidy in recurrent spontaneous aborters: the tendency to parental nondisjunction (1984) (23)
Cytogenetics of malignant gliomas: I. The autosomes with reference to rearrangements. (1995) (22)
Bone marrow monosomy 7: Hematologic and clinical manifestations in childhood and adolescence (1984) (21)
Risks of hematologic malignancy with constitutional chromosome abnormalities. (1987) (21)
Hereditary intestinal neurofibromatosis. I. A distinctive genetic disease. (1988) (21)
Nonreciprocal chromosome translocation t(5;14) in cancers of the kidney: adenocarcinoma of the renal parenchyma and transitional cell carcinoma of the kidney pelvis. (1985) (21)
Amniocyte clones for prenatal cytogenetics. (1981) (20)
Detection of the fragile X chromosome and other fragile sites (1984) (20)
Incidence of major chromosome abnormalities in children. (1977) (20)
Robertsonian chromosome recombinants are rare in cancer. (1988) (20)
Rare, polymorphic, and common fragile sites: a classification (1986) (20)
Genetics of familial neuroblastoma: long-range studies. (1982) (20)
Fragile sites update. (1988) (19)
Incontinentia pigmenti: occurrence in Arizona Indians and evidence against the half-chromatid mutation model. (1982) (19)
Sacrococcygeal teratoma: Prenatal diagnosis with elevated alphafetoprotein and acetylcholinesterase in amniotic fluid (1982) (18)
HUMAN EMBRYONIC HAEMOGLOBINS. (1964) (18)
Nuclear anomalies of the neutrophil in a chromosomal triplication: the D1 (13-15) trisomy syndrome. An electron microscopic study. (1966) (18)
Recognition of neurofibromatosis before von Recklinghausen. (1989) (18)
Of fragile sites and cancer chromosome breakpoints. (1988) (18)
Chromosome changes connect immunodeficiency and cancer in ataxia-telangiectasia. (1987) (17)
Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+). (1971) (17)
Position effect in 8;14 translocation in Burkitt's lymphoma. (1981) (16)
Who will survive with trisomy 13 or 18? A call for cases 10 years old or above. (1981) (16)
The human sex ratio: increase in first-born males to parents with shared HLA-DR antigens. (2008) (16)
IgA and partial deletions of chromosome 18. (1969) (16)
Updating a diagnosis. The EEC/EECUT syndrome. (1985) (16)
Autosomal fragile sites and cancer. (1984) (16)
Unexpected encounters in cytogenetics: repeated abortions and parental sex chromosome mosaicism may indicate risk of nondisjunction. (1982) (16)
Ataxia-telangiectasia breakpoints in chromosome rearrangements reflect genes important to T and B lymphocytes. (1985) (16)
Fragile sites at 4q23 and 7q11.23 unique to bone marrow cells. (1988) (15)
Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication. (1972) (15)
A 1.5-megabase restriction map surrounding MYC does not include the translocation breakpoint in familial renal cell carcinoma. (1989) (15)
Hereditary intestinal neurofibromatosis. II. Translocation between chromosomes 12 and 14. (1988) (15)
The fragile site hypothesis of cancer. (1988) (14)
Chromosome anomalies. (1967) (14)
Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14. (1988) (14)
Oncogene location update. (1988) (13)
Seizure disorders in the fragile X chromosome syndrome. (1991) (13)
The half chromatid mutation model and bidrectional mutation in incontinentia pigmenti (1983) (13)
OVARIAN TERATOMAS AND GENETICS OF GERM-CELL FORMATION (1976) (12)
Genetic control over fragile X chromosome expression (1986) (12)
Detection of fragile sites on human chromosomes. (1985) (12)
Chromosome translocations in cancer. (1981) (12)
Cytogenetics of malignant gliomas. II. The sex chromosomes with reference to X isodisomy and the role of numerical X/Y changes. (1995) (12)
THE NO. 17-18 (E) TRISOMY SYNDROME. STUDIES ON CYTOGENETICS, DERMATOGLYPHICS, PATERNAL AGE, AND LINKAGE. (1963) (12)
Colored reverse-banding of human chromosomes with acridine orange following alkaline/formalin treatment: Densitometric validation and applications (1974) (11)
Genetic activity and fragile sites. (1991) (11)
Observations on the natural history of 49,XXXXY individuals. (1982) (11)
Neurofibromatosis (von Recklinghausen disease). Genetics, cell biology and biochemistry. (1982) (11)
Adenocarcinoma of the gallbladder: chromosome abnormalities in a genetic form of cancer. (1983) (11)
Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3. (1997) (11)
Fibrous histiocytoma cell line: chromosome studies of mouse and man. (1983) (11)
The congenital agammaglobulinemias. A heterogeneous group of immune defects. (1967) (11)
The Placenta in Trisomy 18 Syndrome: Report of 2 Cases (1963) (10)
Ovarian teratomas: cytologic data. (1976) (10)
Chromosome sublocalization of a cDNA for human DNA polymerase-β to 8p11→p12 (1988) (10)
Chromosome analysis in hematologic disorders. The leukemias. (1984) (10)
Inducing fragile sites to express themselves. (1980) (10)
Hematologic malignancy breakpoint update. (1988) (10)
Chromosomes in familial neuroblastoma (1981) (10)
The origin of isochromosomes (1988) (10)
Fragile sites and X-linked retardation. (1981) (10)
Caution about chorionic villi sampling in the first trimester. (1984) (10)
Detection of the X-chromatin body in human fibroblasts by quinacrine fluoromicroscopy. (1971) (10)
Unstable chromosomes in heritable tumor syndromes. Multiple endocrine neoplasia type 1 (MEN1) (1991) (10)
Genetic diagnosis in the newborn. A part of preventive medicine. (1970) (9)
Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis (1989) (9)
Forebrain cleavage gene causing holoprosencephaly: deletion mapping to chromosome band 2p21. (1991) (9)
Enigmatic fragile sites on human chromosomes. (1988) (9)
Human Y-chromatin. I. Dispersion and condensation. (1973) (9)
Guidelines for the diagnosis of fragile X (1986) (9)
Inheritance of giant pigmented hairy nevus of the scalp. (1981) (9)
An acquired Robertsonian translocation in prolymphocytic leukemia: a case presentation and review. (1987) (9)
Chromosome 9 abnormalities in childhood T-cell leukemia. (1986) (9)
Enhanced expression of chromosome fragile site 10q25 in chronic myelogenous leukemia. (1985) (9)
Biologic agents and induction of chromosome fragile sites. (1991) (9)
Little heads: inheritance and early detection. (1979) (9)
2 – The Human Cell Nucleus: Quinacrine and Other Differential Stains in the Study of Chromatin and Chromosomes (1974) (8)
The annals of cancer genetics. The description by Norris of hereditary malignant melanoma of the skin in 1820. (1989) (8)
Genetic issues in public health and medicine. (1979) (8)
LEUKAEMIA AND CHROMOSOME 21 (1982) (8)
Meiotic evidence in Down's syndrome for 21/21 chromosome translocation or isochromosome. (1970) (8)
Position effect in translocation (2;8) in acute lymphocytic leukemia with kappa light chain immunoglobulin expression. (1983) (8)
Invited editorial comment on the article by Salamanca‐Gómez et al: Environmental chromosome damage (1987) (8)
Nuclear abnormalities of neutrophils in the D1 trisomy syndrome (1964) (8)
Chromosome 9 in acute lymphoblastic leukemia: breaks in band 9p21-22 and a fragile site. (1986) (8)
Interchromosomal effects in man (1977) (8)
Inversion of chromosome 5 long arm in region of cell growth gene cluster in hematologic disorders. (1988) (8)
Chromosomal Localization of the Heterochromatic Region 16qh(.76) linked to α-Haptoglobin in Man (1971) (8)
The telomere in cancer. All's not well that doesn't end well. (1991) (8)
Unexpected lambda chain expression in lymphocytic malignancy. (1985) (8)
Human centromere mapping using teratoma data. (1976) (8)
A (1;15) translocation, balanced, 46 chromosomes. Repository identification No. GM-126. (1975) (8)
Fragile sites on chromosomes. (1982) (8)
Neurofibromatosis and malignancy. (1979) (8)
Autosomal rings and variable phenotypes (1973) (7)
Embryonal origin of adult tumors: carcinomas of kidney, bladder, prostate, and testicle. (1987) (7)
Human chromosome breakage: microscopy versus photomicroscopy. (1968) (7)
Transformation of Blood Lymphocytes in Ataxia telangiectasia (1970) (7)
Prenatal diagnosis of a de novo unbalanced translocation (4p + ) following in vitro fertilization (1988) (7)
The Interregional Cytogenetic Register System (ICRS). (1978) (7)
ORAL CLEFTS AND CHILDHOOD CANCER (1980) (7)
The human teratomas: Experimental and clinical biology (1984) (7)
Familial cancer syndromes: catalog with comments (2007) (7)
A mother with Down's syndrome and her chromosomally normal infant. (1971) (7)
Antibiotics containing trimethoprim and the fragile X chromosome. (1983) (7)
Cape Malay hypospadias/mental retardation syndrome. (1988) (7)
CHROMOSOMALLY MARKED LYMPHOCYTE CLONES IN ATAXIA-TELANGIECTASIA (1974) (7)
Fragile X-linked mental retardation of macro-orchidism. (1982) (6)
Telomeric fusion in pre-T-cell acute lymphoblastic leukemia (1986) (6)
Clonal evolution in atypical chronic granulocytic leukemia: a non-Philadelphia translocation. (1978) (6)
Minireview: Rare and polymorphic fragile sites and cancer (1988) (6)
Nonrandom chromosome breakpoints in 6q deletions (1992) (6)
Fetal loss after chorionic villus sampling (CVS) in small and large centres. (1985) (6)
The Philadelphia (Ph) chromosome in leukemia. I. A new mechanism due to interstitial deletion and insertion in chronic myelocytic leukemia. (1985) (6)
Nomenclature: the Philadelphia chromosome or Ph without superscript. (1985) (6)
Exclusion gene mapping utilizing patients with chromosome imbalance: The HL-A system as a prototype (1975) (6)
The Philadelphia (Ph) chromosome in leukemia. III. Complex Ph translocation plus inversion in chronic myelocytic leukemia. (1985) (6)
Establishment and characterization of a common acute lymphoblastic leukemia cell line with a deletion of chromosome 3 band q26. (1987) (6)
Fragile sites and genitourinary tumors. (1988) (5)
Trisomy and disomy in tumors. (1995) (5)
Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature. (1993) (5)
Location of FRAXD in Xq27.2. Fragile sites on the X chromosome. (1990) (5)
Complex cytogenetic findings in acute leukemia. (1983) (5)
INTERFERON-INDUCIBLE FRAGILE SITE ON CHROMOSOME 16 (1981) (5)
Screening for cancer genes. (1992) (5)
Fragile X Gene (1991) (5)
Human Y-chromatin. II. DNA replication. (1973) (5)
Trisomy 21 (Down syndrome): Research perspectives. (1981) (5)
Wiedemann-Beckwith syndrome: cancer predisposition and chromosome 11. (1986) (5)
Neurofibromatosis: Phenotype, natural history, and pathogenesis (1987) (5)
T-cell cancer breakpoints at genes for T-cell receptor on chromosomes 7 and 14. (1986) (5)
Letters to the Editors:Fragile sites and chromosome breakpoints in constitutional rearrangements (1985) (5)
Hemoglobin-Seattle (alpha-2 beta-2 76-Glu): an unstable hemoglobin causing chronic hemolytic anemia. (1970) (4)
Autosomal fragile sites not a current indication for prenatal diagnosis (2004) (4)
Breast cancer, Miss America, and fragile sites. (1993) (4)
The radiologic phenotype of the D1 trisomy syndrome. Abnormalities of the ribs and pelvis. (1965) (4)
Environmental chromosome damage. (1987) (4)
Prenatal Diagnosis of Fragile (X) Syndrome (1984) (4)
New translocations in human lymphocytes: a mutagen monitoring system. (1979) (4)
On the origins of cancer genetics and cytogenetics. (1987) (4)
Re‐evaluation of the effect of spray adhesives on human chromosomes (1976) (4)
Association of a chromatin mass with the fluorescent Y-body in human interphase nuclei. (1972) (4)
Genetic rearrangements in leukaemia and lymphoma (1987) (4)
Jérôme Lejeune (1926–94): In Memoriam. (1994) (4)
Cleft lip and palate: Aspects of reproductive biology. (1988) (4)
Familial hypersensitivity to insect stings. (1971) (4)
Transformation of blood lymphocytes in ataxia telangiectasia. Dose and time response to phytohemagglutinin. (1970) (4)
Bes, Aesop and Morgante: reflections of achondroplasia (1990) (3)
Human afflictions and chromosomal aberrations (1970) (3)
Thalidomide Babies (1962) (3)
Rejoinder to Dr. Daker (1983) (3)
Leukemia and chromosomes. (1974) (3)
45,X/46,XY chromosome mosaicism detected by midtrimester amniocentesis in amniocyte clones (1982) (3)
Immunoglobulin expression in Burkitt's lymphoma and leukemia. (1982) (3)
Uncommon children and common care. (1981) (3)
Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. (1975) (3)
Genetic history: I. The Schneersons of Lubavich (1987) (3)
Human chromosome variation with two Robertsonian translocations (2004) (3)
Cardiomyopathy associated with systemic myopathy. Genetic defect of actomycin influencing muscular structure and function (1979) (3)
[Letters to nature] (1975) (3)
Population cytogenetics of autosomal fragile sites (1986) (3)
DIAGNOSTIC RADIATION AND CHROMOSOME ABERRATIONS (1977) (3)
The consequences of the Philadelphia chromosome rearrangement in chronic myeloid leukemia (2004) (3)
A common toothbrush for dysmorphology. (1979) (3)
Registry of data on Robertsonian (centric-fusion) translocations. (1972) (3)
Maternal cell contamination mooted by amniocyte clones. (1984) (3)
Nonrandom sex chromosome changes in brain tumors. (1994) (3)
9p trisomy identified by Giemsa-11 (1976) (3)
Human cytogenetic registers. A description of nine systems together with some recommendations. (1977) (2)
Chromosomal localization of the heterochromatic region 16qh(.76) linked to alpha-haptoglobin in man. (1971) (2)
Antimutagenesis and anticarcinogenesis mechanisms (1987) (2)
Contemporary management of lymphoma: chromosome studies. (1984) (2)
Familial sex chromosome mosaicism (yes) and interchromosomal effects (no) (1981) (2)
Clonal selection: in the beginning a cell was chosen. (1992) (2)
Human cytogenetic registers. A description of nine systems together with some recommendations. (1977) (2)
Genetic disorders among Jewish people (1980) (2)
Behavior in Klinefelter syndrome, or where there is smoke there may not be a fire. (1990) (2)
Human Gene Mapping 10 (1989): Tenth International Workshop on Human Gene Mapping. Cytogenetic Cell Genet 51:1–1148. (1990) (2)
Human centromere mapping using teratoma data. (1976) (2)
DNA ligase I, Bloom's syndrome, and cancer. (1988) (2)
Descent into demonology and protectionism. (1992) (2)
Agent A. Genetics and litogens. (1987) (2)
TRISOMY 21 OR 22 IN DOWN'S SYNDROME ? (1967) (2)
Rare and polymorphic fragile sites and cancer. (1988) (2)
Lymphocyte culture failure due to toxic tubes. (1982) (2)
Mechanisms of Giemsa banding (1980) (2)
The fragile X chromosome mental retardation and large testes. (1980) (2)
Human heredity, Principles and issues: Michael R. Cummings, West Publishing Company, 1988. $40.00 (US), $44.50 (elsewhere) (xxiii + 476 pages) ISBN 0 314 64032 0 (1989) (2)
Translocation basis for polychromosomal rings. (1995) (2)
Acute leukemic infiltration of the small bowel diagnosed by suction biopsy (1963) (2)
At highest risk: Environmental hazards to young and unborn children. (1980) (2)
Linkage group I: multipoint mapping. (1975) (2)
The mystery of the stable chromosome with two centromeres. (1986) (2)
Animal cancer research. (1991) (1)
Names in genetics: ban on partial trisomy, tetrasomy and monosomy (1986) (1)
The New York Times: "all the news that's fit to print" about medicine and science? (1992) (1)
Chromosome instability before cancer therapy. (1992) (1)
Parental chromosome 11 alleles in Wilms tumor. (1988) (1)
Genetic linkage and physical mapping of a cancer gene. Ataxia-telangiectasia. (1990) (1)
Clinical cytogenetics. Dawn breaks on a new era. (1973) (1)
ABSENCE OF RIB IN DOWN'S SYNDROME (1965) (1)
Nuclear Projections of Neutrophils in the D (13-15) Trisomy Syndrome (1965) (1)
CYTOLOGIC EVIDENCE FOR POSITIOH EFFECT IN BURKITT'S LYMPHOMA (1977) (1)
Chromosome sublocalization of a cDNA for human DNA polymerase-beta to 8p11----p12. (1988) (1)
Teaching medical genetics and Alice in Wonderland. (1981) (1)
Predominance of hemoglobin Gower 1 in early human embryonic life (1966) (1)
REACTIVITY OF MATERNAL LYMPHOCYTES TO PHYTOHÆMAGGLUTININ (1972) (1)
Tort liability in genetic diagnosis and genetic counseling. (1982) (1)
Prenatal diagnosis: Cell biological approaches (1984) (1)
Medical genetics. Part 1: The rise in chromosome abnormalities with maternal age, information for patients and physicians. (1982) (1)
Cytogenetics and Human Neoplasia (1989) (1)
The fetus and the newborn. Annual review of birth defects, 1980. (1982) (1)
Alzheimer's et al. (1990) (1)
Duty to disclose to family members in medical genetics. (1992) (1)
Biomedical research: ethics and rights. (1975) (1)
The molecular cytogenetics of colon cancer. (1988) (1)
GENETIC COUNSELLING IN SPINAL MUSCULAR ATROPHIES (1980) (1)
Total loss of chromosome 17 and p53 gene in solid cancers. (1991) (1)
Perinatology Begins before Conception (1975) (1)
A New Solution to Procreation (1983) (1)
Revolutionary cytogenetics. (1971) (1)
Leukemia and Chromosomes (1974) (1)
Congenital chromosome abnormalities and cancer. (1983) (1)
Genetic heterogeneity of ataxia‐telanglectasia (1989) (1)
At increased risk: neural tube defect relatives. (1983) (1)
Antenatal and neonatal screening. (1985) (1)
Advantages of amniocyte clones for prenatal cytogenetics (1982) (1)
In memory yet green. The autobiography of Isaac Asimov, 1924-1953 (1979) (1)
Linkage of skeletal dysplasia gene to t(2;8)(q32;p13) chromosome translocation breakpoint. (1984) (1)
Partial trisomy 15 (dup 15q) syndrome and the need for precision in clinical cytogenetics (1975) (1)
Mild mental retardation with unusual features including cataracts, hyperostosis frontalis interna, oligomenorrhea, and dislocating patellae (MR/CHOP) (1976) (1)
The nature of non-disjunction. (1990) (1)
Letter: Partial trisomy 15 (dup15q) syndrome and the need for precision in clinical cytogenetics. (1975) (1)
Down syndrome: Growing and learning. (1979) (1)
Newborn infants with Hb Portland 1, an indicator of alpha-chain deficiency. (1968) (1)
Letter: Chromosomally marked lymphocyte clones in ataxia-telangiectasia. (1974) (1)
Recent advances and new syndromes. (1979) (1)
Webster's New World medical dictionary : from the doctors and experts at MedicineNet.com (2003) (1)
Mara and Benomi Buck: familial mental retardation in colonial Jamestown. (1973) (1)
ALCOHOLIC CIRRHOSIS IN ASHKENAZI JEWS AND HLA (1982) (1)
Contemporary management of leukemia: cytogenetic diagnosis and monitoring of chronic myelocytic leukemia. (1981) (0)
Cross currents in human genetics (1983) (0)
Immunogenetics and immunology: I. key to the future. (1981) (0)
Progressive tenosynovitis with contractures and possible systemic involvement--a new heritable disorder of connective tissue? (1975) (0)
Know your genes (1980) (0)
At increased risk: Down syndrome relatives. (1983) (0)
The True History of the Elephant Man (1981) (0)
Editorial help (2004) (0)
Genetic intelligence: William Frederick Friedman, cryptanalyst-a speculative note. (1971) (0)
Cis-trans position effect in cancer translocations. (1984) (0)
Thoughts on a manuscript (1989) (0)
Ocular manifestations of De Lang syndrome (1975) (0)
Down syndrome. A comprehensive bibliography. (1981) (0)
Catalog of chromosome aberrations in cancer. (1988) (0)
Sewall Wright, 98, top geneticist. (1988) (0)
To band, or not to band? (1982) (0)
1942-11-25, Frederick to Family (1942) (0)
Immunologic markers in the diagnosis of the acute lymphocytic leukemias. (1982) (0)
Contents, Vol. 39, 1970 (1970) (0)
Murder of son with a genital malformation. (1995) (0)
Guidelines Should Cover Illustrations Too (1992) (0)
References to the committee reports (1975) (0)
Chromosomes in Hematology. Edited by R. Becher, A. A. Sandberg, and C. G. Schmidt. W. Zuckschwerdt Verlag: Munich and San Francisco, 1986, pp. 171. (1987) (0)
Subject Index Vol. 16, 1976 (1976) (0)
1942-01-24, Frederick to Family (1942) (0)
Down's syndrome. Mongolism and its management. By Clemens E. Benda. Grune and Stratton, New York. 279 pp. 1969 (1971) (0)
Sam latt: Pioneer in molecular cytogenetics (1988) (0)
Malpractice Issues (1984) (0)
First-trimester prenatal diagnosis by trophoblast biopsy. (1983) (0)
Book ReviewChromosomes and Cancer. (1975) (0)
Gene symbols for fragile sites: a proposal (1989) (0)
NEW CHROMOSOMAL AND MALFORMATION SYNDROMES (1975) (0)
Principles and practice of pediatric oncology, edited by Philip A. Pizzo and David G. Poplack, 1989, 1129 pages, J. B. Lippincott, Philadelphia, $125.00. (1989) (0)
Chromosomes and cancer. (1980) (0)
“Unstable” translocation not proven unstable (1989) (0)
Antibodies CD20.2 and CD20.3 bind to and activate several human B cell lines (1996) (0)
D1 trisomy syndrome, leukemia, and immunologic abnormalities (1968) (0)
Ataxia-telangiectasia: the primary defect? (1978) (0)
Limiting eponyms (cont'd) (1984) (0)
Utilization of immunogenetics and cytogenetics in the diagnosis of leukemias and lymphomas (1983) (0)
Advances in Medical Genetics: Huntington Disease (1987) (0)
Human chromosomes: Structure, behavior, effects By E. Therman. New York: Springer-Verlag. (1986). 313 pp. $29.80 (1987) (0)
Advances in medical genetics: Huntington disease. (1987) (0)
patient, they may return to favor, just as have wigs, long hair, tight trousers and beards." (1979) (0)
Contemporary management of leukemia: cytogenetic diagnosis and monitoring of acute leukemia and preleukemia. (1981) (0)
Linkage group I: multipoint mapping. (1975) (0)
Genetics: Human aspects (1983) (0)
Dynamic genetic counseling for clinicians (1971) (0)
Light upon the origin of leukemia. (1984) (0)
Ovarian teratomas: cytologic data. (1976) (0)
Elements of medical genetics (1980) (0)
1942-09-01, Frederick to Marie (1942) (0)
Part II: genetics and obstetrics. The early detection of high-risk pregnancies with maternal serum AFP testing. (1982) (0)
Sex differentiation and chromosomal abnormalities (1979) (0)
High birth defect rates in Arizona? Geographic and ethnic factors bearing upon late childbearing and birth defect rates. (1983) (0)
Sex chromosome aneuploidy: Prospective studies on children. (1979) (0)
Down's syndrome (Mongolism). (1971) (0)
White, Unused Paper (WUP) in Pediatrics (1974) (0)
A cytogenetical analysis in patients with secondary hematological disorders. (1987) (0)
THE AUTOSOMAL TRISOMIES (1964) (0)
Book ReviewMolecular Structure of Human Chromosomes. (1978) (0)
Why am I...? A new thought on genetics (1982) (0)
Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. (1975) (0)
LEUKÆMIA IN MOTHER AND CHILD (1959) (0)
Letter to the Editor (1982) (0)
The Nijmegen Breakage Syndrome. Clinical, Immunological, Cytogenetic and Cellbiological Studies, be Rob Taalman. 153 pp., 1987. Nijmegen, Krips Repro Meppel (1988) (0)
Malpractice and women 35 years of age or more at delivery. (1982) (0)
Family chromosome studies. (1971) (0)
Testosterone-binding protein probably not Y-linked. (1971) (0)
Mapping the gene for X-linked lymphoproliferative disease. (1990) (0)
Perfecting the world. The life and times of Dr. Thomas Hodgkin 1798–1866,: by Amalie M. Kass and Edward H. Kass, 1988, Boston, Harcourt Brace Jovanovich, $34.95. (1990) (0)
Genetic history: II. The Cohens of London (1987) (0)
The tricentennial people: Human applications of the new genetics (1979) (0)
Genetics in Pediatrics (1987) (0)
Environmental causes of human birth defects. (1990) (0)
A tribute to Dr. Bilderback—“Dr. Bil” (1970) (0)
Book ReviewHuman Chromosomes (1976) (0)
Chromosomes and Cancer (1977) (0)
Book Review Index Vol. 10, 1971 (1971) (0)
Cell surface factors, immune deficiencies, twin studies (1979) (0)
Genetic and Related Biomedical Aspects of Twinning (1983) (0)
Phenotypic differentiation of autosomal chromosomal abnormalities. Anomalies on the gross, radiologic, autopsy, cellular, and molecular levels in the D-1 (13-15) trisomy syndrome. (1966) (0)
1941-02-07, Military Appointment Card (1941) (0)
21/21 translocation: Correlation of banding with meiotic results (1973) (0)
Contents Vol. 118, 2007 (2007) (0)
Occasional comment: Genentech and George Hardy (1981) (0)
Human somatic cell metaphase chromosome measurements. (1994) (0)
Subject Index Vol. 10, 1971 (1971) (0)
HOMOGRAFTS IN CHORIONEPITHELIOMA (1963) (0)
Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia Cell Lines without Classical Breakpoint Cluster Region Rearrangement 1 (2006) (0)
Genetics in the Courts, by Henry M. Butzel. Volume 9 in Studies in Health and Human Services, 801 pp., 1987. Queenston, Ontario, Canada, The Edwin Mellen Press (1988) (0)
Chromosome analysis guidelines - preliminary report (2016) (0)
Case studies in genetics. (1979) (0)
To draw a new line. (1970) (0)
The genetics of fetal wastage (1983) (0)
Agent B. Genetics and litogens. (1990) (0)
Genetics in clinical oncology (1986) (0)
Fetal trimethadione toxicity: an historical footnote. (1979) (0)
Frederick Hecht Correspondence #02 (1941) (0)
Creativity in medical genetics and dysmorphology. (1991) (0)
Letter to the editor (0)
The poisoned womb (1987) (0)
Couples with repeat spontaneous abortions: chromosome abnormalities. (1984) (0)
Kamus kedokteran : Webster's new world (2010) (0)
Two Problems: Diagnosing the EEC/EECUT Syndrome and Recommending Dietary Fiber-Reply (1986) (0)
724 MAPPING THE HLA GENE CLUSTER WITH PARTHENOGENIC OVARIAN TERATOMAS (1981) (0)
X-LINKED IMMUNOCOMPETENCE AND EPSTEIN-BARR VIRUS ONCOGENESIS (1979) (0)
Genetics and cancer: chromosomes and oncogenes. (1983) (0)
Sex chromosome conversion from XY to monosomy X to XX in brain tumor cells (1994) (0)
Are geneticists born or made? The issue of training and certification (1983) (0)
Aneuploidy, non-disjunction, and chromosome 21 (1990) (0)
Medical genetics: Principles and practice (1975) (0)
A taste for death (1987) (0)
From The Broken Cord (2020) (0)
An oncogenic cast to the chromosomes. (1993) (0)
Risks with translocation in "typus edinburgensis". (1992) (0)
The malformed infant and child. An illustrated guide (1984) (0)
Editorial correspondenceGenetic counseling (1985) (0)

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