Orlando Jack Miller
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Biology
Orlando Jack Miller's Degrees
- Masters Biology Stanford University
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(Suggest an Edit or Addition)Orlando Jack Miller's Published Works
Number of citations in a given year to any of this author's works
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
- Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. (1977) (1346)
- A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA (1985) (630)
- Suppression of human nucleolus organizer activity in mouse-human somatic hybrid cells. (1976) (441)
- The chromosomes in a patient showing both mongolism and the Klinefelter syndrome. (1959) (308)
- Expression of human and suppression of mouse nucleolus organizer activity in mouse-human somatic cell hybrids. (1976) (307)
- 5-Methylcytosine localised in mammalian constitutive heterochromatin (1974) (264)
- Frequency of satellite association of human chromosomes is correlated with amount of Ag-staining of the nucleolus organizer region. (1977) (144)
- Serologic detection of a y-linked gene in xx males and xx true hermaphrodites. (1976) (140)
- Nucleolus organizers in Mus musculus subspecies and in the RAG mouse cell line. (1977) (123)
- Chromosome localization of highly repetitive human DNA's and amplified ribosomal DNA with restriction enzymes. (1983) (121)
- The organization of the mouse satellite DNA at centromeres. (1989) (111)
- Mapping the locus of the H-Y gene on the human Y chromosome. (1977) (111)
- The 13q-deletion syndrome. (1969) (108)
- A family with an XXXXY male, a leukaemic male, and two 21-trisomic mongoloid females. (1961) (103)
- Human Thymidine Kinase Gene Locus: Assignment to Chromosome 17 in a Hybrid of Man and Mouse Cells (1971) (100)
- Human chromosome 19 carries a poliovirus receptor gene (1974) (96)
- Suppression of production of mouse 28S ribosomal RNA in mouse-human hybrids segregating mouse chromosomes. (1977) (93)
- Quinacrine fluorescent karyotypes of human diploid and heteroploid cell lines. (1971) (89)
- Identification of the mouse karyotype by quinacrine fluorescence, and tentative assignment of seven linkage groups. (1971) (88)
- Erythroid cell differentiation: murine erythroleukemia cell variant with unique pattern of induction by polar compounds. (1976) (86)
- Expression of H-Y antigen in human males with two Y chromosomes. (1975) (85)
- The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-). (1970) (83)
- Amplified ribosomal RNA genes in a rat hepatoma cell line are enriched in 5-methylcytosine. (1981) (75)
- Chromosome structure as revealed by a combined chemical and immunochemical procedure. (1973) (75)
- Eukaryotic chromosome replication. (1988) (74)
- NON-RANDOM DISTRIBUTION OF CHROMOSOMES IN METAPHASE FIGURES FROM CULTURED HUMAN LEUCOCYTES. I. THE PERIPHERAL LOCATION OF THE Y CHROMOSOME. (1963) (73)
- Sexual and somatic determinants of the human Y chromosome: studies in a 46,XYp- phenotypic female. (1979) (73)
- H–Y antigen and the origin of XY female wood lemmings (Myopus schisticolor) (1976) (72)
- Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas (1997) (72)
- THE SEX CHROMOSOME ANOMALIES. (1964) (70)
- Consistent pattern of binding of anti-adenosine antibodies to human metaphase chromosomes. (1972) (68)
- Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families. (1967) (64)
- NON-RANDOM DISTRIBUTION OF CHROMOSOMES IN METAPHASE FIGURES FROM CULTURED HUMAN LEUCOCYTES. II. THE PERIPHERAL LOCATION OF CHROMOSOMES 13, 17-18 AND 21. (1963) (61)
- The use of antinucleoside antibodies to probe the organization of chromosomes denatured by ultraviolet irradiation. (1974) (60)
- Relationship of mouse minor satellite DNA to centromere activity. (1990) (59)
- Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers). (1972) (59)
- Localization of 5-methylcytosine in human metaphase chromosomes by immunoelectron microscopy (1976) (56)
- Mitotic separation of two human X-linked genes in man--mouse somatic cell hybrids. (1971) (55)
- Detection of nucleolus organizer regions in chromosomes of human, chimpanzee, gorilla, orangutan and gibbon (1976) (55)
- A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas. (1996) (54)
- The gorilla karyotype: chromosome lengths and polymorphisms. (1974) (52)
- Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients. (1970) (51)
- Identification of translocation chromosomes by quinacrine fluorescence. (1972) (50)
- A human alpha satellite DNA subset specific for chromosome 12. (1990) (49)
- Evidence for methylation of inactive human rRNA genes in amplified regions (1981) (48)
- Human–mouse cell hybrid with human multiple Y chromosomes (1976) (48)
- A male with XXYY chromosomes (1961) (47)
- Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15 (2004) (47)
- Chromosome analysis of two related heteroploid mouse cell lines by quinacrine fluorescence. (1973) (47)
- OBSERVATIONS ON CHROMOSOME DUPLICATION IN CULTURED HUMAN LEUCOCYTES. (1963) (46)
- Human chromosome structure as revealed by an immunoperoxidase staining procedure. (1974) (46)
- Chromosome markers in Mus musculus: strain differences in C-banding. (1973) (43)
- The quinacrine fluorescence karyotype of Mus musculus and demonstration of strain differences in secondary constrictions. (1971) (43)
- Mutations in the arginine-rich protein gene, in lung, breast, and prostate cancers, and in squamous cell carcinoma of the head and neck. (1996) (42)
- Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome. (1966) (41)
- Complement deficiency and chromosomalbreaks in a case of Swiss-type agammaglobulinaemia. (1968) (40)
- Spreading of inactivation in an (X;14) translocation. (1978) (40)
- Chromosome Mapping in the Mouse (1972) (40)
- Restriction enzyme banding of mouse metaphase chromosomes (2004) (39)
- Method for locating the centromeres of mouse meiotic chromosomes and its application to T163H and T70H translocations. (1972) (38)
- Q- and C-band chromosome markers in inbred strains of Mus musculus. (1976) (38)
- Chromosome analysis and alkaline phosphatase of C41, a cell line of human cervical origin distinct from HeLa. (1977) (36)
- Chromosomal translocations in patients with mongolism and in their normal relatives. (1962) (35)
- Binding of anti-nucleoside antibodies reveals different classes of DNA in the chromosomes of the kangaroo rat (Dipodomys ordii). (1977) (35)
- Nucleolus organizer activity and the origin of Robertsonian translocations. (1978) (35)
- 5-Methylcytosine in heterochromatic regions of chromosomes: chimpanzee and gorilla compared to the human (1975) (35)
- A human alphoid DNA clone from the EcoRI dimeric family: genomic and internal organization and chromosomal assignment. (1989) (34)
- Distinction between chromosome 4 and chromosome 5 by replication pattern and length of long and short arms. (1967) (33)
- Quinacrine Fluorescence Patterns of Human D Group Chromosomes (1971) (33)
- Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas (1997) (32)
- Report of the committee on the genetic constitution of chromosomes 10, 11, 12, X, and Y. (1980) (32)
- The quinacrine fluorescent and Giemsa banding karyotype of the rat, Rattus norvegicus, and banded chromosome analysis of transformed and malignant rat liver cell lines. (1972) (30)
- Chromosomes and cancer in the mouse: studies in tumors, established cell lines, and cell hybrids. (1983) (30)
- Familial translocation involving chromosome 6, 14 and 20, identified by quinacrine fluorescence (2004) (30)
- The c-myc oncogene is translocated to the involved chromosome 12 in mouse plasmacytoma. (1985) (29)
- Overabundance of rare-cutting restriction endonuclease sites in the human genome. (1987) (28)
- Regulation of rRNA gene expression in a human familial 14p+ marker chromosome (1978) (28)
- Dermatoglyphic features of patients with a partial short arm deletion of a B‐group chromosome (1967) (27)
- Karyotype of the gibbons hylobates lar and h. moloch inversion in chromosome 7. (1975) (27)
- Autoradiography in human cytogenetics. (1970) (27)
- Human chromosomes in 18 man-mouse somatic hybrid cell lines analysed by quinacrine fluorescence. (1973) (26)
- Cytological detection of the c-25H deletion involving the albino (c) locus on chromosome 7 in the mouse. (1974) (26)
- Is DNA methylation responsible for mammalian X chromosome inactivation? (1982) (26)
- Human tumor and rodent-human hybrid cells with an increased number of active human NORs. (1978) (26)
- Demonstration of Increased Gonadotrophic Hormone Production in Castrated Mice with Intrasplenic Ovarian Grafts.∗ (1950) (25)
- Mutations in the arginine-rich protein gene (ARP) in pancreatic cancer (1997) (25)
- Application of new staining techniques to the study of human chromosomes. (1973) (24)
- Banded chromosomes of the owl monkey, Aotus trivirgatus. (1977) (24)
- DELETED LATE-REPLICATING CHROMOSOME 4/5 (1966) (24)
- Report of the Committee on the Genetic Constitution of the X and Y Chromosomes. (1984) (24)
- Mapping the locus of the H-Y antigen. (1976) (23)
- Clusterine in deleted short-arm length among 25 cases with a Bp-chromosome. (1969) (23)
- Distinctive fluorescence of quinacrine-labelled human G group chromosomes. (1971) (23)
- Reaction of antinucleoside antibodies with human cells in vitro. (1971) (23)
- Giemsa banding of chromosomes. (1972) (22)
- Ag-staining of nucleolus organizer regions of chromosomes after A-,C-, G-, or R-banding procedures. (1977) (22)
- Pattern of undermethylation of the major satellite DNA of mouse sperm. (1985) (22)
- Isolation and comparative mapping of a human chromosome 20-specific α-satellite DNA clone (1992) (22)
- Chromosomal heterogeneity in the RAG and MSWBS mouse tumor cell lines. (1974) (22)
- Chromosome markers in Mus musculus: Differences in C-banding between the subspecies M. m. musculus and M. m. molossinus (1975) (21)
- Assignment of four linkage groups to chromosomes in Mus musculus and a cytogenetic method for locating their centromeric ends. (1971) (21)
- Transcription and processing of both mouse and Syrian hamster ribosomal RNA genes in individual somatic hybrid cells. (1978) (21)
- Chromosome-specific subsets of human alphoid DNA identified by a chromosome 2-derived clone. (1990) (21)
- Antibodies to histones and histone-histone complexes: immunochemical evidence for secondary structure in histone 1 (1976) (20)
- Location of rRNA genes in three inbred strains of rat and suppression of rat rRNA activity in rat-human somatic cell hybrids. (1979) (20)
- Marked increase in ribosomal RNA gene multiplicity in a rat hepatoma cell line (1979) (19)
- Autoradiographic Studies of X-chromosome Duplication in an XO/X-isochromosome X Mosaic Human Female (1963) (19)
- A chimpanzee-derived chromosome-specific alpha satellite DNA sequence conserved between chimpanzee and human (1991) (19)
- Genome composition and tandemly repetitive sequence at some centromeres in the lizard Podarcis s. sicula Raf. (2004) (19)
- Cytogenetics of the mouse. (1975) (18)
- Sex Determination and the Y Chromosome (2001) (18)
- Autoradiographic studies on a mother and aborted foetus from a family with four mongoloid children and a presumptive 21/21 translocation (1968) (18)
- p82H identifies sequences at every human centromere (1987) (17)
- Identification by quinacrine fluorescence of the chromosome carrying mouse linkage group I in the Cattanach translocation. (1971) (17)
- Occurrence and evolution of homogeneously staining regions may be due to breakage-fusion-bridge cycles following telomere loss (2004) (17)
- Sex Determination: The Sex Chromosomes and the Sex Chromatin Pattern (1962) (16)
- Translocation of centromeric heterochromatin in the T(10;13) 199H stock of Mus musculus and localization of chromosome break points. (1974) (16)
- 5-Methylcytosine in heterochromatic regions of chromosomes in Bovidae (1976) (16)
- Spontaneous cell hybridization of somatic cells present in sperm suspensions. (1976) (16)
- Relationship between the number and function of human ribosomal genes (1988) (16)
- Karyotype of Friend virus-induced mouse erythroleukemia cells (1979) (16)
- Time of suppression of human rRNA genes in mouse-human hybrid cells. (1979) (16)
- Isolation of a variant family of mouse minor satellite DNA that hybridizes preferentially to chromosome 4. (1991) (15)
- CHROMOSOME DUPLICATION IN CULTURED LEUCOCYTES FROM PRESUMPTIVE XXX AND XXXXY HUMAN SUBJECTS. (1964) (15)
- 5-Methylcytosine in the DNA of the polytene chromosomes of the dipteraSciara coprophila,Drosophila melanogaster andD. persimilis (2005) (15)
- SECTION OF BIOLOGICAL AND MEDICAL SCIENCES: I. NORMAL VARIATIONS IN THE HUMAN KARYOTYPE* (1962) (15)
- Lamin A/C gene and a related sequence map to human chromosomes 1q12.1-q23 and 10 (1993) (14)
- H-Y antigen in 46,XY gonadal dysgenesis (2004) (14)
- Detection of minute deletions in human karyotypes. (1969) (14)
- Quinacrine fluorescence of Mus cervicolor chromosomes. Bright centrometric heterochromatin. (1973) (14)
- Gonadoblastoma occurring in a female with XO-XY fragment gonadal dysgenesis. (1971) (13)
- Quinacrine fluorescence patterns and terminal DNA labelling of human C group chromosomes. (1972) (13)
- Human ribosomal DNA fragments amplified in hamster cells are transcribed only by RNA polymerase II and are not silver stained. (1987) (13)
- Polymorphism of 5-methylcytosine-rich DNA in human acrocentric chromosomes (2004) (13)
- The rat XC sarcoma cell line: ribosomal RNA gene amplification and banded karyotype. (1982) (13)
- Partial deletion of short arm of chromosome no. 4. (1971) (12)
- Recent developments in human cytogenetics. (1961) (12)
- Assignment of linkage groups 8 and X to chromosomes in Mus musculus and identification of the centromeric end of linkage group I. (1971) (12)
- Retinoblastoma and partial deletion of the long arm of chromosome 13. (1978) (12)
- Transcription of mouse rDNA and associated formation of the nucleolus organizer region after gene transfer and amplification in Chinese hamster cells (1985) (12)
- GONADAL DYSGENESIS (TURNER'S SYNDROME) WITH MALE PHENOTYPE AND XO CHROMOSOMAL CONSTITUTION (1960) (12)
- Radioautographic identification of the D chromosomes involved in the centric fusion type of D/G translocation, t(DqGq) (1968) (11)
- Meiosis in Arthroderma benhamiae (=Trichophyton mentagrophytes). (1968) (11)
- Human semen as a source of epithelial cells for culture (1978) (11)
- Nucleic acid-reactive antibodies specific for nucleosides and nucleotides. (1972) (11)
- The organization of DNA in the mitotic and polytene chromosomes of Sciara coprophila (2004) (11)
- Autosomal chromosome disorders and variations. (1976) (11)
- Methylation of the 5′ flanking sequences of the ribosomal DNA in human cell lines and in a human‐hamster hybird cell line (1992) (11)
- The role of thyroid function and food intake in experimental ovarian tumorigenesis in mice. (1954) (11)
- Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
- Isolation of large numbers of chromosome 3-specific cosmids containing clusters of rare restriction-endonuclease sites. (1991) (10)
- Inverse relationship between transcriptional activity and 5-methylcytosine content of DNA in polytene chromosomes of sciara coprophila. (1981) (10)
- Presumptive C-15 translocation and familial large Y identified by autoradiography. (1969) (10)
- Human Chromosomes (2001) (10)
- Absence of somatic pairing of sex chromatin masses (inactivated X chromosomes) in cultured cells from a human XXXXY male. (1967) (9)
- The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3. (1992) (9)
- "PURE" GONADAL DYSGENESIS WITH XO/XX MOSAICISM. (1964) (9)
- The structural organization of mouse metaphase chromosomes (1977) (8)
- The fifties and the renaissance in human and mammalian cytogenetics. (1995) (8)
- Nucleolar organisers in mammalian cells (1981) (8)
- Asynchronous DNA Replication and Discordant Length of Homologous Autosomes demonstrated by the Use of Markers (1968) (8)
- Animal cytology and evolution (1974) (8)
- Further evidence of X-linkage of hypoxanthine phosphoribosyl-transferase in the mouse. (1976) (8)
- Restriction Enzyme Banding of Metaphase Chromosomes (1990) (7)
- Generation of human B‐cell hybridomas secreting monoclonal anti–myelin‐associated glycoprotein antibodies from a patient with neuropathy (1987) (7)
- Genetic correction of hereditary disease. (1989) (7)
- Sex determination: the sex chromosomes and the sex chromatin pattern. (1962) (7)
- Sendai virus-induced cell sorting leading to apparent preferential fusion of like cells. (1971) (6)
- Quinacrine fluorescent chromosome analysis of the Snell translocation in the mouse. (1972) (6)
- Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
- The Mitotic Cell Cycle (2001) (6)
- Isolation and comparative mapping of a human chromosome 20-specific alpha-satellite DNA clone. (1992) (6)
- The control of sex chromatin. I. The significance of the distribution of sex chromatin counts in individuals with three or more X chromosomes. (1968) (6)
- Comparative mapping of a gorilla-derived alpha satellite DNA clone on great ape and human chromosomes (1991) (6)
- The control of sex chromatin (1968) (6)
- Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
- Autoradiographic studies of chromosomes 4 and 5 in the cri du chat syndrome (1965) (5)
- Assignment of human thymidine kinase gene locus to chromosome 17 by identification of its distinctive quinacrine-fluorescence in man/mouse somatic hybrid cells (1971) (5)
- Traditional and molecular cytogenetics. (1992) (5)
- Report of the committee on the genetic constitution of chromosomes 10, 11, and 12. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (5)
- The role of trypsin in the pre-treatment of chromosomes for giemsa banding (1976) (5)
- Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
- Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
- Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
- Quinacrine fluorescent patterns of the chromosomes in cell lines of the rat-kangaroo (Potorous tridactylus apicalis). (1971) (4)
- The biarmed Mus poschiavinus chromosome carrying the H-2 locus, T1posKlj, IS T7Bnr. (1972) (4)
- Chromosome changes in cell differentiation. (1997) (4)
- Increased intracellular phosphoribosylpyrophosphate and accelerated orotic acid decarboxylation in a mouse cell line resistant to purine and pyrimidine ribonucleosides (1977) (4)
- Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
- [Chromosome aberrations in a case of Turner's syndrome]. (1963) (4)
- Anopthalmia and Other Anomalies Associated with a Ring Chromosome No. 17-18 (1975) (3)
- Absence of nucleolar dominance in mouse-human heterokaryons. (1981) (3)
- Report of the committee on the genetic constitution of the X and Y chromosomes. (1976) (3)
- Is the centromeric heterochromatin ofMus musculus late replicating? (1976) (3)
- Present Status and Future Trends in Prenatal Diagnosis of Chromosomal Disorders (1972) (3)
- Isolation and characterization of a mouse subtelomeric sequence (1992) (3)
- Seven genes on the short arm of human chromosome 3 map to two regions on Macropus eugenii (tammar wallaby) chromosome 2. (1994) (3)
- Isolation of two contigs of overlapping cosmids derived from human chromosomal band 3p21.1 and identification of 5 new 3p21.1 genes (1994) (3)
- Immunological Approaches for the Detection of DNA Modified by Environmental Agents (1983) (3)
- Report of the committee on the genetic constitution of chromosomes 10, 11, and 12. (1982) (2)
- Genome Destabilization and Multistep Progression to Cancer (2001) (2)
- The mouse chromosome map. (1975) (2)
- Nylon-fiber affinity selection of red blood cells and tissue culture cells on the basis of cell surface determinants. (1980) (2)
- Autoradiographic study of DNA synthesis in homologous chromosomes distinguishable by morphology. (1971) (2)
- Immunochemical probes of chromosome organization. (1976) (2)
- Immunochemical studies on the 5-methylcytosine content of African green monkey satellite DNA. (1978) (2)
- Immunochemical probes of human chromosome organization. (1975) (2)
- Replication pattern and quinacrine fluorescence of the chromosomes of a CV-1-derived African green monkey cell line. (1973) (1)
- Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
- Clinical Importance of Translocations, Inversions, and Insertions (2001) (1)
- Prenatal Sex-Chromatin and Chromosome Analysis (1968) (1)
- Genetic counseling: meeting today's and tomorrow's needs. (1970) (1)
- ABH blood group antigens on cultured epithelial cells. (1980) (1)
- Human cytogenetic registries (1975) (1)
- The Causes of Structural Aberrations (2001) (1)
- Homogeneously staining regions (HSRs) of a rat hepatoma cell line are not early replicating. (1985) (1)
- Mapping the locus of the H-Y antigen. (1976) (1)
- DNA methylation is not increased in mouse-human somatic cell hybrids. (1985) (1)
- Human Genetic Mutant Cell Repository Index / Book Review Index (1974) (1)
- DNA, chromatin and chromosomes (1983) (1)
- Chromosomes in cystic fibrosis. (1968) (1)
- Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
- XY Gonadal Dysgenesis and Gonadoblastoma: Report of a Case (1969) (1)
- CHROMOSOMAL CAUSES OF INTERSEXUALITY (1967) (1)
- General Features of Mitotic Chromosomes (2001) (1)
- Structure and organization of mammalian chromosomes: normal and abnormal. (1987) (1)
- First announcement of the Fanconi Anemia International Registry (1982) (1)
- Dermatoglyphic features of patients with a partial short arm deletion of a B‐group chromosome* (1967) (0)
- Use of antibodies to nucleosides and nucleotides in studies of nucleic acids in cells. (1975) (0)
- DNA and Gene Amplification (2001) (0)
- In Situ Hybridization (2001) (0)
- Cytogenetics of the Mammalian X Chromosome. Part B: Chromosome Anomalies and Their Clinical Manifestations. Progress and Topics in Cytogenetics, Volume 3B.Avery A. Sandberg (1985) (0)
- Subject Index Vol. 13, 1974 (1974) (0)
- Somatic Cell Hybridization in Cytogenetic Analysis (2001) (0)
- Syndromes Due to Autosomal Deletions and Duplications (2001) (0)
- Chromosomenaberrationen bei einem Turner-Fall (2004) (0)
- Human Genetic Mutant Cell Repository Index Vol. 18, 1977 (1977) (0)
- Anopthalmia and other anomalies associated with a ring chromosome No. 17 approximately 18. (1975) (0)
- Contents, Vol. 37, 1984 (1984) (0)
- Human chromosomes DNA synthesis (1971) (0)
- Report of the committee on the genetic constitution of the x and y chromosomes. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (0)
- Mapping Human Chromosomes (2001) (0)
- Updating advances in cytogenetics. (1974) (0)
- Methods in human cytogenetics. (1975) (0)
- Contents, Vol. 32, 1982 (1982) (0)
- Chromosome analysis in infertility. (1961) (0)
- [5-Methylcytosine as a specific building block of heterochromatin in man]. (1975) (0)
- Book Review Index Vol. 10, 1971 (1971) (0)
- [Behavior of mitochondria in virus-induced hybrids from cells with varying mitochondrial structure]. (1975) (0)
- Prenatal Sex-Chrotnatin and Chron1oso1ne Analysis (1968) (0)
- DNA and chromosomes. (1971) (0)
- The X Chromosome, Dosage Compensation, and X Inactivation (2001) (0)
- Bibliography of Ulrich Wolf (2001) (0)
- Report of the committee on the genetic constitution of chromosomes 10, 11, 12, X, and Y. (1979) (0)
- Somatic cell genetics (2014) (0)
- Subject Index Vol. 32, 1982 (1982) (0)
- Subject Index Vol. 10, 1971 (1971) (0)
- Comparative mammalian cytogenetics (1970) (0)
- Meiotic Abnormalities: Abnormal Numbers of Chromosomes (2001) (0)
- Contents, Vol. 65, 1994 (1994) (0)
- Gene therapy. (1987) (0)
- Phenotypic Effects of Sex Chromosome Imbalance (2001) (0)
- Discussion of Dr. Croce’s Paper (1977) (0)
- The Future of Human Cytogenetics (2001) (0)
- Abnormal Phenotypes Due to Autosomal Aneuploidy or Polyploidy (2001) (0)
- Congenital chromosome anomalies. (1978) (0)
- Studies on granulosa cell tumors occurring in intrasplenic ovarian grafts in castrate mice (1950) (0)
- Subject Index Vol. 20, 1978 (1978) (0)
- Deleted late-replicating chromosomes. (1966) (0)
- Catalog of mapped human gene markers. (1980) (0)
- Report of the committee on the genetic constitution of the X and Y chromosomes. (1982) (0)
- News and notices (2005) (0)
- Basel to Freiburg: a journey worth taking (2000) (0)
- Contents, Vol. 18, 1977 (1977) (0)
- Genome Plasticity and Chromosome Evolution (2001) (0)
- Contents Vol. 91, 2000 (2001) (0)
- DNA Replication and Chromosome Reproduction (2001) (0)
- Meiotic confirmation of the identification of chromosomes 9 and 13 in T(9; 19)163H, T(5; 13)264 Ca, and T(1; 13)70H stocks in Mus musculus (2004) (0)
- Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
- Contents, Vol. 4, Supplement 1, 1989 (1989) (0)
- Contents, Vol. 13, 1974 (1974) (0)
- News and notices (2005) (0)
- Human Genetics Molecular Structure of Human Chromosomes Jorge J. Unis (1979) (0)
- Standard nomenclature applies to cell lines too. (1981) (0)
- [Chromosome findings in gynecology]. (1961) (0)
- Subject Index Vol. 25, 1979 (1979) (0)
- Prenatal Sex-Chromatin and Chrollloso11le Analysis (1968) (0)
- Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
- Subject Index Vol. 91, 2000 (2000) (0)
- Advanced techniques in chromosome research (1992) (0)
- The diagnosis of chromosome abnormalities in newborn infants by the use of umbilical cord blood cultures. I. Mongolism. (1961) (0)
- Partial deletion o/the short arm of chromosome No 4(4t,-). Clinical ,t,di , i, unrelated patients (1970) (0)
- Identification of human translocation chromosomes by quinacrine fluorescence patterns (1971) (0)
- Subject Index Vol. 65, 1994 (1994) (0)
- Euploid Chromosome Aberrations, Uniparental Disomy, and Genomic Imprinting (2001) (0)
- HumanRibosomal DNA Fragments Amplified inHamsterCells AreTranscribed OnlybyRNA Polymerase II and AreNotSilver Stained (1987) (0)
- Atlas of Human Chromosomes Clinical Atlas of Human Chromosomes Jean de Grouchy Catherine Turleau (1979) (0)
- Chromosomes and Cancer: Activation of Oncogenes (2001) (0)
- Fragile Sites, Trinucleotide Repeat Expansion, and the Fragile X Syndrome (2001) (0)
- Subject Index Vol. 22, 1978 (1978) (0)
- Human ribosomal DNA fragments amplified in hamster cells are transcribed only by RNA polymerase II and are not silver stained (1987) (0)
- Subject Index Vol. 16, 1976 (1976) (0)
- Molecular Correlates of Chromosome Bands (2001) (0)
- Peter John Langford Cook, BA, MB Cantab., PhD Lond. (1982) (0)
- Chromosomes and Cancer: Inactivation of Tumor Suppressor Genes (2001) (0)
- Magnification and Regulation of Ribosomal Genes in Normal Cells and Cancer Cells (2008) (0)
- Standard chromosome nomenclature (1981) (0)
- Symposium on intrauterine diagnosis. Discussion of symposium papers. (1971) (0)
- Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
- Book Review:Human Afflictions and Chromosomal Aberrations. Raymond Turpin, Jerome Lejeune (1971) (0)
- The Chemistry and Packaging of Chromosomes (2001) (0)
- Dosage compensation in mammals: Why does a gene on the inactive X yield less product than one on the active X? (2004) (0)
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