John L. Hamerton
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Biology
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(Suggest an Edit or Addition)John L. Hamerton'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
- A colchicine, hypotonic citrate, squash sequence for mammalian chromosomes. (1956) (752)
- A cytogenetic survey of 14,069 newborn infants (1975) (386)
- A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. (1976) (265)
- Prenatal diagnosis of genetic disease in Canada: report of a collaborative study. (1976) (226)
- Standardization in human cytogenetics (2004) (170)
- The cytogenetics of mammalian autosomal rearrangements. (1989) (135)
- Chromosome translocation as a cause of familial mongolism. (1960) (117)
- Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis: Final report (1992) (111)
- Chromosome studies in a neonatal population. (1972) (102)
- Robertsonian translocations in man: evidence for prezygotic selection. (1968) (102)
- Chromosome Polymorphism in the Common Shrew (1957) (100)
- Chromosome studies in detection of parents with high risk of second child with Down's syndrome. (1961) (96)
- Human genes encoding prothrombin and ceruloplasmin map to 11p11–q12 and 3q21–24, respectively (1987) (89)
- CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS. (1965) (87)
- Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor (1985) (85)
- Familial mental retardation in a family with an inherited chromosome rearrangement (1974) (75)
- Genetic intersexuality in goats. (1969) (75)
- Significance of Sex Chromosome Derived Heterochromatin in Mammals (1968) (72)
- THE SOMATIC CHROMOSOMES OF THE HOMINOIDEA. (1963) (67)
- Chromosomal Mosaicism in Diagnostic Amniotic Fluid Cell Cultures (1974) (66)
- Chromosomal changes in primary and transplanted reticular neoplasms of the mouse. (1958) (66)
- Sex-chromosome Abnormalities in a Population of Mentally Defective Children (1962) (63)
- A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations. (1978) (61)
- Cytogenetic and endocrine studies of a freemartin heifer and its bull co-twin. (1969) (59)
- Differential transmission of Down's syndrome (mongolism) through male and female translocation carriers. (1961) (58)
- THE LONDON CONFERENCE ON THE NORMAL HUMAN KARYOTYPE, 28TH-30TH AUGUST, 1963. (1963) (56)
- Report of the Committee on the Genetic Constitution of Chromosome (1974) (54)
- An international system for human cytogenetic nomenclature (1978) ISCN (1978). Report of the Standing Commitee on Human Cytogenetic Nomenclature. (1978) (50)
- Down syndrome and recent demographic trends in Manitoba. (1978) (48)
- A FAMILY SHOWING TRANSMISSION OF A D/D RECIPROCAL TRANSLOCATION AND A CASE OF REGULAR 21-TRISOMIC DOWN'S SYNDROME. (1963) (46)
- IVth International Workshop on Human Gene Mapping (1977) (43)
- CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES. (1965) (40)
- Deletion of the short arm of chromosome No. 10. (1975) (37)
- Structural gene encoding human factor XII is located at 5q33-qter (1988) (36)
- The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7 (1989) (35)
- Localization of the gene encoding human factor V to chromosome 1q21-25. (1988) (34)
- Non-random X Chromosome Expression in Female Mules and Hinnies (1971) (33)
- Sex chromatin and human chromosomes. (1961) (33)
- CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). II. THE FREQUENCY OF INTERCHANGE TRISOMY IN PATIENTS BORN AT A MATERNAL AGE OF LESS THAN 30 YEARS. (1965) (33)
- Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis (1982) (33)
- CHROMOSOMES IN MEDICINE (1962) (31)
- Paris Conference (1971), supplement (1975) Standardization in human cytogenetics. (1975) (31)
- Chromosome Findings in Chronic Psychotic Patients (1968) (30)
- 56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy site (1983) (29)
- Report of the committee on the genetic constitution of chromosome 1. (1979) (29)
- Chorionic villus sampling and amniocentesis for prenatal diagnosis (1997) (29)
- Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR. (1990) (28)
- G6PD Expression and X Chromosome Late Replication in Fibroblast Clones from a Female Mule (1972) (27)
- Isolation and characterization of an α-satellite repeated sequence from human chromosome 22 (2004) (26)
- Report of the Committee on the Genetic Constitution of Chromosome 1. (1978) (26)
- Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes. (1991) (26)
- Regional localization of 18 human X-linked DNA sequences. (1986) (25)
- Localization of human gene loci using spontaneous chromosome rearrangements in human-Chinese hamster somatic cell hybrids. (1975) (24)
- Characteristics of an HPRT-deficient chinese hamster cell line. (1974) (23)
- Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22. (1986) (23)
- Somatic Chromosomes of the Gorilla (1961) (23)
- Books and Monographs (1969) (23)
- Human cytogenetics : general cytogenetics (1971) (22)
- PROGENY OF D/G TRANSLOCATION HETEROZYGOTES IN FAMILIAL DOWN'S SYNDROME (1962) (22)
- DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21. (1987) (22)
- Immunogenetics of sex determination of the polled goat. (1980) (22)
- Isolation and characterization of a processed gene for human ceruloplasmin. (1987) (22)
- Regional localization of loci for human PGM and 6PGD on human chromosome one by use of hybrids of Chinese hamster-human somatic cells. (1973) (21)
- Chromosomal localization and structure of the human P1 protamine gene. (1989) (20)
- The association of glucose phosphate isomerase expression with human chromosome 19 using somatic cell hybrids (1973) (18)
- The gene for clotting factor 10 is mapped to 13q32----qter. (1986) (18)
- Physical and psychologic parameters in children with sex chromosome anomalies: further follow-up from the Winnipeg Cytogenetic Study of 14,069 newborn infants. (1986) (17)
- A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the children with sex chromosome anomalies. (1982) (17)
- A DNA marker for human chromosome 8 that detects alleles of differing sizes. (1986) (17)
- Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man. (1976) (16)
- Report of the Committee on Chromosome Markers. (1975) (16)
- DETECTION AND CROSS‐REACTION OF H‐Y ANTIGEN BY HAEMAGGLUTINATION (1978) (16)
- Confirmation of the assignment of MYCL to chromosome 1 in humans and its position relative to RH, UMPK, and PGM1. (1988) (15)
- Biochemical investigations in cultured skin fibroblasts from patients with Duchenne muscular dystrophy (1978) (15)
- C-band polymorphisms of chromosomes 1, 9, and 16 in four subgroups of mentally retarded patients and a normal control population (1979) (14)
- Tertiary trisomy 14: is there a syndrome? (1976) (13)
- Human Radiation Cytogenetics (1968) (13)
- Assignment of three human gene loci to regions of chromosome 2. (1975) (13)
- Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR). (1991) (12)
- ISOZYME ANALYSIS OF SOMATIC CELL HYBRIDS: ASSIGNMENT OF THE PHOSPHOGLUCOMUTASE 2 ( PGM 2 ) GENE LOCUS TO CHROMOSOME 4 IN MAN WITH DATA ON THE MOLECULAR STRUCTURE AND HUMAN CHROMOSOME ASSIGNMENTS OF SIX ADDITIONAL MARKERS (1975) (12)
- A 48,XXXX female (1974) (12)
- Mapping the human 5S RNA genes on chromosome 1 using translocations. (1975) (12)
- Fetal sex. (1970) (12)
- Policy statement concerning DNA banking and molecular genetic diagnosis. Canadian College of Medical Geneticists. (1991) (11)
- Homozygous Robertsonian translocations in a fetus with 44 chromosomes (1982) (11)
- An intersex goat with a bilaterally asymmetrical reproductive tract. (1968) (11)
- Limb defects and chorionic villus sampling (1996) (11)
- Paris Conference (1971): standardization in human cytogenetics. (1972) (11)
- Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
- Collaborative studies in prenatal diagnosis of chromosome aberrations (1984) (10)
- A summary of the human gene map, 1973-1977. (1978) (10)
- Human population cytogenetics: dilemmas and problems. (1976) (10)
- The Chromosome Disorders. An Introduction for Clinicians (1967) (10)
- Evidence for the role of the maternal immune system in balancing the sex ratio in mice. (1980) (9)
- Investigation of the origin of variant, truncated estrogen receptor-like mRNAs identified in some human breast cancer biopsy samples (2004) (9)
- Special Notice to Contributors and Subscribers (1976) (9)
- Chapter 6 – ABNORMALITIES OF THE AUTOSOMES–GROUP E (16–18 GROUP–DENVER CONFERENCE) (1971) (9)
- Proline incorporation by cultured skin fibroblasts from patients with Duchenne muscular dystrophy (1982) (9)
- Cytogenetic characteristics of 26 polyethylene glycol-induced human-hamster hybrid cell lines. (1979) (9)
- Prenatal diagnosis in Canada — 1990: A review (1994) (9)
- Human gene mapping 4 : Winnipeg conference (1977), fourth International Workshop on Human Gene Mapping (1978) (8)
- Searching for Molecular Abnormalities in Genetic Diseases by the Use of a Double Labeling Technique. II. Deficiency of a Basic Protein in Fibroblasts of Patients with Pompe's Disease (1978) (7)
- Banding patterns of metaphase chromosomes in Down's syndrome. (1971) (7)
- Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter→q21 (1980) (7)
- Children and young adults with sex chromosome aneuploidy : follow-up, clinical, and molecular studies : proceedings of the 5th International Workshop on Sex Chromosome Anomalies held at Minaki, Ontario, Canada, June 7-10, 1989 (1991) (7)
- Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man. (1976) (7)
- Chapter 2 – ABNORMAL SEX CHROMOSOME COMPLEMENTS IN THE FEMALE (1971) (6)
- Non-random Inactivation of the X Chromosome in the Female Mule (1970) (6)
- A MONGOL CHILD WITHOUT TRISOMY G. (1965) (6)
- Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
- Chapter 5 – AUTOSOMAL ABNORMALITIES–GROUP G (1971) (6)
- A BglII RFLP at the human prolactin gene locus on chromosome 6 (PRL). (1991) (6)
- Report of the committee on the genetic constitution of chromosomes 1 and 2. (1975) (6)
- Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
- Sex chromosome anomalies: prenatal diagnosis and the need for continued prospective studies. (1990) (5)
- Chapter 9 – CYTOGENETICS OF HUMAN PREGNANCY WASTAGE (1971) (5)
- Proceedings: Synteny of the IDH-1 and MDH-1 gene loci in man and probable assignment to chromosome 2. (1974) (5)
- DOWN'S SYNDROME (MONGOLISM) WITH NORMAL CHROMOSOMES (1962) (5)
- Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
- Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
- Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
- Antenatal diagnosis of neural tube defects in Canada: extension of a collaborative study. (1979) (5)
- Mapping the human 5S RNA genes on chromosome 1 using translocations. (1975) (5)
- 4 – MAMMALIAN SEX CHROMOSOMES (1958) (5)
- Analyses of data on rates of cytogenetic disorders in live births. (1978) (5)
- Constitutive heterochromatin in mouse chromosomes treated with typsin. (1973) (5)
- Human chromosomes control growth of human-chinese hamster somatic cell hybrids (1982) (4)
- The effect of gamma irradiation of human cells and somatic cell hybridization on sister chromatid exchange frequencies in the hamster chromosomes of hamster-human hybrid lines. (1981) (4)
- Localization of the processed gene for human ceruloplasmin to chromosome region 8q21.13----q23.1 by in situ hybridization. (1988) (4)
- Cytogenetic disorders. (1984) (4)
- Chapter 3 – THE SEX CHROMOSOMES AND INTERSEXUALITY IN MAN (1971) (4)
- TaqI and RsaI RFLP's at the prolactin inducible protein (PIP) locus on chromosome 7. (1989) (4)
- The effects of gamma irradiation of human fibroblasts on human/Chinese hamster somatic cell hybrids. (1981) (4)
- Chapter 10 – CHROMOSOMES AND NEOPLASTIC DISEASE (1971) (4)
- Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome (1991) (4)
- The H-Y antigen:production of antibodies, detection, and cross-reaction between mouse, rat, and human. (1978) (4)
- Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
- Defining the chromosomal basis of mental handicap (1999) (4)
- The characteristics of a population of Canadian women offered maternal serum alphafetoprotein screening during pregnancy. (1986) (3)
- Section 2: Chromosome disease (1981) (3)
- Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons. (1992) (3)
- Heterogeneity in the biochemical characteristics of red blood cell hypoxanthine-guanine phosphoribosyl transferase from two unrelated patients with the lesch-nyhan syndrome (1973) (3)
- Conformation of the assignment of a glutathione peroxidase locus to chromosome 3 in man. (1979) (3)
- Proceedings: Localization of the structural gene for human peptidase-A to chromosome 18. (1974) (3)
- A ribulose 5-phosphate 3-epimerase (RPE) locus is on human chromosome 2. (1982) (3)
- Translocation in Human Chromosomes with Special Reference to Mental Retardation and Congenital Malformations (1968) (3)
- Human phosphoglycolate phosphatase is coded by a gene on chromosome 16. (1980) (3)
- Workshop on collaborative studies in prenatal diagnosis of chromosome disease. (1982) (2)
- Chapter 8 – ABNORMALITIES OF THE AUTOSOMES: TRISOMICS, DELETIONS, DUPLICATIONS, AND TRANSLOCATIONS (EXCEPT GROUPS D, E, AND G) (1971) (2)
- Physical and psychological findings in adolescents with sex chromosome abnormalities ascertained in the Winnipeg Cytogenetic Study of Newborns: 1970-1973. (1990) (2)
- Proposed banding nomenclature for the Chinese hamster chromosomes (Cricetulus grises). (1976) (2)
- Human cytogenetic registries (1975) (2)
- Chapter 4 – SEX DETERMINATION AND THE SIGNIFICANCE OF THE SEX CHROMOSOME ABNORMALITIES IN MAN AND MAMMALS (1971) (2)
- Clonal culture of human amniocytes. (1982) (2)
- Assignment of the inorganic pyrophosphatase gene locus (PP) to chromosome 10 in man. (1976) (2)
- Intracellular Localization of Four Dehydrogenases in Human Skin Fibroblasts in Tissue Culture (1964) (2)
- Chromosomal localization of a sequence with in vivo activity for initiation of DNA replication (1993) (2)
- Report of the committee on the genetic constitution of chromosome 1. (1982) (2)
- Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter leads to q21. (1980) (2)
- Tentative assignment of the peptidase-A (Pep-A) gene locus to the (q21-qter) region of chromosome 18 in man. (1975) (2)
- Human Population Cytogenetics (1968) (1)
- Localization of gene loci on chromosome 12 and the X in man. (1975) (1)
- Chicago Conference 1966: Standardization in Human Cytogenetics (1967) (1)
- Ethical considerations in newborn chromosome screening programs. (1979) (1)
- Localization of gene loci on chromosome 12 and the X in man. (1975) (1)
- Demonstration of fluorescent X and Y bodies after antibody- and complement-mediated cytotoxicity (1977) (1)
- Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
- Further data on the assignment of the phosphoglucomutase2 (PGM2) gene locus to chromosome 4 in man. (1975) (1)
- Long-term lymphocyte cultures--cytogenetics. (1973) (1)
- Assignment of three human gene loci to regions of chromsome 2. (1975) (1)
- CHORIONIC VILLUS SAMPLING VERSUS AMNIOCENTESIS (1989) (1)
- Report of the committee on the genetic constitution of chromosome 1. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (1)
- Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
- Familial chromosomal aberrations and metabolic disorders. (1992) (1)
- Tentative assignment of the peptidase-A (Pep-A) gene locus to the (q21 leads to qter) region of chromosome 18 in man. (1975) (1)
- Rapide Mbeddinogf Minuteo Bjectisn Paraffin (1956) (1)
- Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
- Subject Index Vol. 22, 1978 (1978) (0)
- References to the committee reports (1975) (0)
- [No Title] (1969) (0)
- Cardiomyopathy in duchenne/becker muscular dystrophy: Gene analysis with DNA probesclose to the disease locus * (1986) (0)
- Incorporation of methionine sulphur into cysteine in vitro by fibroblasts deficient in cystathionine synthetase. (1969) (0)
- Note to contributors and readers (1974) (0)
- Contents, Vol. 37, 1984 (1984) (0)
- Human Cytogenetics (1961) (0)
- The William Allan Memorial Award. Presented to Patricia A. Jacobs, D.Sc., at the annual meeting of the American Society of Human Genetics, Dallas, October 28-31, 1981. (1982) (0)
- Assignment of the inorganic chromosome 10 in man. (1976) (0)
- Deletion of the Long Arms of Chromosome 18 (46,XX,18q-) Associated with Absence of IgA and Hypothyroidism in an Adult (2006) (0)
- Books and Monographs (1968) (0)
- Fetal karyotype of amniotic cells without culturing. (1972) (0)
- The human complement after trypsin pretreatment as compared to the Paris standard (1975) (0)
- Report of the committee on the genetic constitution of chromosome 1. (1980) (0)
- Regional localizations of four markers on chromosome 1 using a 1/4 translocation. (1976) (0)
- Contents, Vol. 32, 1982 (1982) (0)
- Subject Index Vol. 32, 1982 (1982) (0)
- Characterization of cDNA Clones Corresponding to Genomic Loci Rearranged in Patients with Prader-Willi Syndrome (1992) (0)
- Painter, Theophilus Schickel (2001) (0)
- Contents, Vol. 24, 1979 (1974) (0)
- Obituary (1888) (0)
- Catalog of mapped human gene markers. (1980) (0)
- Chromosomes and Genes. The Biological Basis of Heredity (1970) (0)
- The Handling of Chromosomes (1970) (0)
- Proceedings: Report of the Committee on the Genetic Constitution of Chromosome 1. (1974) (0)
- THE HUMAN X CHROMOSOME (1962) (0)
- Subject Index Vol. 20, 1978 (1978) (0)
- Sex Chromosomes (1968) (0)
- Annex 8: Familial chromosomal aberrations and metabolic disorders (1992) (0)
- Chromosomes in Medicine (1962) (0)
- The Elements of Cytogenetics (1970) (0)
- Regional localization of four markers on chromosome 1 using 1/4 translocation. (1976) (0)
- Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
- The Genetical Society of Great Britain Abstracts of Papers read at the hundred and fifty-eighth meeting of the Society held on 8th and 9th November 1968, at the University College, London (1969) (0)
- Books and Monographs (1969) (0)
- Two RFLPs identified by an anonymous sequence (D7S19) (pTS119) from chromosome 7. (1987) (0)
- LYONISATION OF THE X CHROMOSOME. (1964) (0)
- The association of glucose phasphate isomerase expression with human chromosome 19 using somatic cell hybrids. (1973) (0)
- The human X chromosome. (1990) (0)
- An Atlas of Mammalian Chromsomes, Vol. 1 (1968) (0)
- Subject Index Vol. 47, 1988 (1988) (0)
- Subject Index Vol. 25, 1979 (1979) (0)
- Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
- Human Afflictions and Chromosome Abberations (1970) (0)
- Contents, Vol. 47, 1988 (1988) (0)
- In Reply: CHROMOSOME ABNORMALITIES IN PSYCHIATRIC PATIENTS (1969) (0)
- Subject Index Vol. 16, 1976 (1976) (0)
- Effects of radiation of human-Chinese hamster somatic cell hybrids (1979) (0)
- Peter John Langford Cook, BA, MB Cantab., PhD Lond. (1982) (0)
- Further data on the assignment of the phosphoglucomutase (PGM2) gene locus to chromosome 4 in man. (1975) (0)
- The Chromosomes of the Hominoidea (2017) (0)
- CHORIONIC VILLUS SAMPLING AND EARLY AMNIOCENTESIS FOR PRENATAL DIAGNOSIS. AUTHORS' REPLY (1997) (0)
- Subject Index Vol. 24, 1979 (1979) (0)
- Chorionic villus sampling and early amniocentesis for prenatal diagnosis (1997) (0)
- Standard chromosome nomenclature (1981) (0)
- Introduction (1981) (0)
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