J. Hamerton

发表

THE LONDON CONFERENCE ON THE NORMAL HUMAN KARYOTYPE, 28TH-30TH AUGUST, 1963.

J. Hamerton, H. Klinger, D. Mutton, 1963, Cytogenetics.

Investigation of the origin of variant, truncated estrogen receptor-like mRNAs identified in some human breast cancer biopsy samples

L. Murphy, J. Hamerton, J. Schwarz, 2004, Breast Cancer Research and Treatment.

Confirmation of the assignment of MYCL to chromosome 1 in humans and its position relative to RH, UMPK, and PGM1.

J. Hamerton, T. Zelinski, P. Mcalpine, 1988, Genomics.

Painter, Theophilus Schickel

J. Hamerton, 2001 .

Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes.

J. Hamerton, A. Chudley, C. Gregory, 1991, American journal of medical genetics.

G6PD Expression and X Chromosome Late Replication in Fibroblast Clones from a Female Mule

J. Hamerton, M. Ray, P. A. Gee, 1972, Nature.

Structural gene encoding human factor XII is located at 5q33-qter

J. Hamerton, R. MacGillivray, N. Royle, 1988, Somatic cell and molecular genetics.

Non-Random Late Replication of X Chromosomes in Mules and Hinnies

J. Hamerton, F. Giannelli, J. L. HAMERTON, 1971, Nature.

A cytogenetic survey of 14,069 newborn infants

J. Hamerton, S. Smith, M. Ray, 1975 .

A colchicine, hypotonic citrate, squash sequence for mammalian chromosomes.

C. E. Ford, J. Hamerton, 1956, Stain technology.

Localization of the gene encoding human factor V to chromosome 1q21-25.

J. Hamerton, R. MacGillivray, E. Guinto, 1988, Genomics.

Localization of the processed gene for human ceruloplasmin to chromosome region 8q21.13----q23.1 by in situ hybridization.

M. Koschinsky, J. Hamerton, H. Wang, 1988, Cytogenetics and cell genetics.

Evidence that the Xg Blood Group Genes are on the Short Arm of the X chromosome

J. Hamerton, J. Lindsten, M. Fraccaro, 1963, Nature.

Assignment of three human gene loci to regions of chromosome 2.

T. Mohandas, J. Hamerton, G. Douglas, 1975, Birth defects original article series.

Localization of human gene loci using spontaneous chromosome rearrangements in human-Chinese hamster somatic cell hybrids.

T. Mohandas, J. Hamerton, J. McAlpine, 1975, American journal of human genetics.

Prenatal diagnosis of genetic disease in Canada: report of a collaborative study.

J. Hamerton, N. Simpson, J. Miller, 1976, Canadian Medical Association journal.

The association of glucose phosphate isomerase expression with human chromosome 19 using somatic cell hybrids

J. Hamerton, G. Douglas, P. A. Gee, 1973 .

A summary of the human gene map, 1973-1977.

J. Hamerton, L. Donald, 1978, Cytogenetics and cell genetics.

DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.

J. Hamerton, C. Greenberg, K. Wrogemann, 1987, American journal of human genetics.

Report of the committee on the genetic constitution of chromosome 1.

J. Hamerton, P. Cook, 1982, Birth defects original article series.

Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man.

T. Mohandas, J. Hamerton, M. Ray, 1976, Cytogenetics and cell genetics.

Mapping the human 5S RNA genes on chromosome 1 using translocations.

J. Hamerton, D. Mutton, W. Prensky, 1975, Birth defects original article series.

Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.

J. Hamerton, C. Greenberg, A. Chudley, 1990, American journal of medical genetics.

Non-random X-Inactivation in the Female Mule

J. Hamerton, R. Short, F. Giannelli, 1969, Nature.

Evidence for the role of the maternal immune system in balancing the sex ratio in mice.

J. Hamerton, A. Shalev, N. A. Nelson, 1980, Journal of reproductive immunology.

Chromosomal localization and structure of the human P1 protamine gene.

J. Hamerton, R. Pon, S. Krawetz, 1989, Genomics.

Isolation and characterization of an α-satellite repeated sequence from human chromosome 22

J. Hamerton, H. McDermid, A. Duncan, 2004, Chromosoma.

Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor

J. Hamerton, J. Parks, R. Mallonee, 1985, Somatic cell and molecular genetics.

Chromosome translocation as a cause of familial mongolism.

J. Hamerton, C. Carter, P. Polani, 1960, Lancet.

Sex chromatin and human chromosomes.

J. Hamerton, 1961, International review of cytology.

An international system for human cytogenetic nomenclature (1978) ISCN (1978). Report of the Standing Commitee on Human Cytogenetic Nomenclature.

J. Hamerton, J. Lindsten, D. Bergsma, 1978, Cytogenetics and cell genetics.

IVth International Workshop on Human Gene Mapping

J. Hamerton, 1977 .

Proline incorporation by cultured skin fibroblasts from patients with Duchenne muscular dystrophy

J. Hamerton, K. Wrogemann, E. Rosenmann, 1982, Journal of the Neurological Sciences.

Chromosomal localization of a sequence with in vivo activity for initiation of DNA replication

J. Hamerton, M. Zannis‐Hadjopoulos, Cunle Wu, 1993, Somatic cell and molecular genetics.

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

T. Mohandas, J. Hamerton, P. McAlpine, 1975 .

Deletion of the short arm of chromosome No. 10.

J. Hamerton, M. Ray, H. O'Brien, 1975, Journal of medical genetics.

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.

J. Hamerton, M. Ray, N. Canning, 1976, Clinical genetics.

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

J. Hamerton, P. Polani, F. Giannelli, 1965, Cytogenetics.

Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis

J. Hamerton, K. Wrogemann, E. Rosenmann, 1982, Nature.

Somatic Chromosomes of the Gorilla

J. Hamerton, H. Klinger, E. Lang, 1961, Nature.

Chromosome Investigations of a Small Isolated Human Population: Chromosome Abnormalities and Distribution of Chromosome Counts According to Age and Sex Among the Population of Tristan Da Cunha

J. Hamerton, R. Angell, V. McGuire, 1965, Nature.

Policy statement concerning DNA banking and molecular genetic diagnosis. Canadian College of Medical Geneticists.

J. Hamerton, R. Korneluk, D. Rosenblatt, 1991, Clinical and investigative medicine. Medecine clinique et experimentale.

Human genes encoding prothrombin and ceruloplasmin map to 11p11–q12 and 3q21–24, respectively

N J Royle, D M Irwin, M L Koschinsky, 1987, Somatic cell and molecular genetics.

Genetic intersexuality in goats.

J. Hamerton, R. Short, S. Grieves, 1969, Journal of reproduction and fertility. Supplement.

Chorionic villus sampling and amniocentesis for prenatal diagnosis

J. Hamerton, L. Stranc, J. Evans, 1997, The Lancet.

Standardization in human cytogenetics

J. Hamerton, 2004, Human Genetics.

Homozygous Robertsonian translocations in a fetus with 44 chromosomes

J. Hamerton, J. Evans, C. Rockman‐Greenberg, 1982, Human Genetics.

Cytological Identification of Radiation-Chimæras

C. E. Ford, J. Hamerton, J. Loutit, 1956, Nature.

Immunogenetics of sex determination of the polled goat.

J. Hamerton, R. Short, A. Shalev, 1980, Cytogenetics and cell genetics.

Cytogenetic and endocrine studies of a freemartin heifer and its bull co-twin.

J. Hamerton, R. Short, E. P. Evans, 1969, Cytogenetics.

Chromosomal Mosaicism in Diagnostic Amniotic Fluid Cell Cultures

J. Hamerton, D. Cox, V. Niewczas-Late, 1974, Pediatric Research.

Human chromosomes control growth of human-chinese hamster somatic cell hybrids

J. Hamerton, L. Donald, H. Wang, 1982, Somatic cell genetics.

The effects of gamma irradiation of human fibroblasts on human/Chinese hamster somatic cell hybrids.

J. Hamerton, L. Donald, N. Holliday, 1981, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

Significance of Sex Chromosome Derived Heterochromatin in Mammals

J. Hamerton, 1968, Nature.

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES.

J. Hamerton, C. Carter, P. Polani, 1965, Cytogenetics.

PROGENY OF D/G TRANSLOCATION HETEROZYGOTES IN FAMILIAL DOWN'S SYNDROME

J. Hamerton, A. Steinberg, J. Hamerton, 1962 .

Differential transmission of Down's syndrome (mongolism) through male and female translocation carriers.

J. Hamerton, V. Cowie, P. Polani, 1961, Lancet.

Chromosome studies in detection of parents with high risk of second child with Down's syndrome.

J. Hamerton, C. Carter, F. Giannelli, 1961, Lancet.

A FAMILY SHOWING TRANSMISSION OF A D/D RECIPROCAL TRANSLOCATION AND A CASE OF REGULAR 21-TRISOMIC DOWN'S SYNDROME.

J. Hamerton, C. Carter, F. Giannelli, 1963, Cytogenetics.

Sex-chromosome Abnormalities in a Population of Mentally Defective Children

J. Hamerton, G. Jagiello, B. Kirman, 1962, British medical journal.

Chromosomal changes in primary and transplanted reticular neoplasms of the mouse.

C. E. Ford, J. Hamerton, R. Mole, 1958, Journal of cellular physiology. Supplement.

4 – MAMMALIAN SEX CHROMOSOMES

J. Hamerton, 1958 .

Chromosome Polymorphism in the Common Shrew

C. E. Ford, J. Hamerton, G. Sharman, 1957, Nature.

Human Radiation Cytogenetics

J. Hamerton, 1968 .

Translocation in Human Chromosomes with Special Reference to Mental Retardation and Congenital Malformations

J. Hamerton, 1968 .

Robertsonian translocations in man: evidence for prezygotic selection.

J. Hamerton, 1968, Cytogenetics.

A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations.

J. Hamerton, A. Hunter, J. Evans, 1978, Cytogenetics and cell genetics.

The cytogenetics of mammalian autosomal rearrangements.

J. Hamerton, 1989 .

Tertiary trisomy 14: is there a syndrome?

J. Hamerton, M. Ray, J. Briggs, 1976, Birth defects original article series.

Heterogeneity in the biochemical characteristics of red blood cell hypoxanthine-guanine phosphoribosyl transferase from two unrelated patients with the lesch-nyhan syndrome

J. Hamerton, B. J. Richardson, D. Ryckman, 1973, Biochemical Genetics.

Mapping the human 5S RNA genes on chromosome 1 using translocations.

J. Hamerton, D. Mutton, W. Prensky, 1975, Cytogenetics and cell genetics.

Report of the Committee on the Genetic Constitution of Chromosome

J. Hamerton, P. Cook, 1974 .

Non-random X Chromosome Expression in Female Mules and Hinnies

J. Hamerton, R. Short, W. Allen, 1971, Nature.

Isolation and characterization of a processed gene for human ceruloplasmin.

M. Koschinsky, J. Hamerton, R. MacGillivray, 1987, Biochemistry.

Familial mental retardation in a family with an inherited chromosome rearrangement

J. Hamerton, A. Chudley, M. Ray, 1974, Journal of medical genetics.

Report of the Committee on the Genetic Constitution of Chromosome 1.

N. Morton, S. Povey, J. Hamerton, 1978, Cytogenetics and cell genetics.

Report of the committee on the genetic constitution of chromosome 1.

J. Hamerton, P. Cook, 1979, Cytogenetics and cell genetics.

Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons.

D. Yan, J. Hamerton, C. Greenberg, 1992, American journal of medical genetics.

Section 2: Chromosome disease

A. Robinson, A. de la Chapelle, J. Hamerton, 1981 .

Chromosome studies in a neonatal population.

J. Hamerton, G. Ducasse, M. Ray, 1972, Canadian Medical Association journal.

Biochemical investigations in cultured skin fibroblasts from patients with Duchenne muscular dystrophy

J. Hamerton, K. Wrogemann, S. Pena, 1978, Clinical genetics.

THE SOMATIC CHROMOSOMES OF THE HOMINOIDEA.

J. Hamerton, H. Klinger, D. Mutton, 1963, Cytogenetics.

Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis: Final report

J. Hamerton, A. Lippman, J. Shime, 1992, Prenatal diagnosis.

Defining the chromosomal basis of mental handicap

J. Hamerton, L. Stranc, 1999, The Lancet.

The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7

J. Hamerton, R. Shiu, C. Gregory, 1989, Somatic cell and molecular genetics.

The Chromosome Disorders. An Introduction for Clinicians

J. Hamerton, 1967 .

Human population cytogenetics: dilemmas and problems.

J. Hamerton, 1976, American journal of human genetics.

Intracellular Localization of Four Dehydrogenases in Human Skin Fibroblasts in Tissue Culture

J. Hamerton, D. Mutton, R. Spector, 1964, Nature.

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

J. Hamerton, C. Gregory, A. J. Kirkilionis, 1991, Human Genetics.

Antenatal diagnosis of neural tube defects in Canada: extension of a collaborative study.

J. Hamerton, N. Simpson, L. Siminovitch, 1979, Canadian Medical Association journal.

Chapter 2 – ABNORMAL SEX CHROMOSOME COMPLEMENTS IN THE FEMALE

J. Hamerton, 1971 .

CHROMOSOMES IN MEDICINE

J. Hamerton, 1962, British medical journal.

Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22.

J. Hamerton, H. McDermid, A. Duncan, 1986, Chromosoma.

Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR).

J. Hamerton, C. Gregory, A. J. Kirkilionis, 1991, Genomics.

Abstracts of meeting presentations (Part 3 of 11)

A. Chapelle, J. Opitz, N. Morton, 1979 .

Chromosome Findings in Chronic Psychotic Patients

J. Hamerton, G. Jagiello, P. Polani, 1968, British Journal of Psychiatry.

[No Title]

J. Hamerton, G. Jagiello, 1969, British Journal of Psychiatry.

Abstracts of meeting presentations (Part 2 of 11)

R. L. Miller, D. Cox, K. Kidd, 1982 .

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

J. Hamerton, K. Wrogemann, S. Pena, 1978, Pediatric Research.

Report of the Committee on Chromosome Markers.

J. Hamerton, 1975, Birth defects original article series.

Regional localization of 18 human X-linked DNA sequences.

L. Mulligan, J. Hamerton, N. Simpson, 1986, Cytogenetics and Cell Genetics.

Proposed banding nomenclature for the Chinese hamster chromosomes (Cricetulus grises).

J. Hamerton, 1976, Birth defects original article series.

Paris Conference (1971), supplement (1975) Standardization in human cytogenetics.

J. Hamerton, H. Klinger, Edwin S. Geffner, 1975, Cytogenetics and cell genetics.

Human cytogenetics : general cytogenetics

J. Hamerton, 1971 .

Familial chromosomal aberrations and metabolic disorders.

J. Hamerton, A. Lippman, L. Dallaire, 1992, Prenatal diagnosis.

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). II. THE FREQUENCY OF INTERCHANGE TRISOMY IN PATIENTS BORN AT A MATERNAL AGE OF LESS THAN 30 YEARS.

J. Hamerton, C. Carter, F. Giannelli, 1965, Cytogenetics.

Chapter 6 – ABNORMALITIES OF THE AUTOSOMES–GROUP E (16–18 GROUP–DENVER CONFERENCE)

J. Hamerton, 1971 .

Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter→q21

J. Hamerton, L. Donald, H. Wang, 1980, Biochemical Genetics.

THE HUMAN X CHROMOSOME

J. Hamerton, 1962, Developmental medicine and child neurology.

C-band polymorphisms of chromosomes 1, 9, and 16 in four subgroups of mentally retarded patients and a normal control population

J. Hamerton, H. Wang, 1979, Human Genetics.

Limb defects and chorionic villus sampling

J. Hamerton, J. Evans, 1996, The Lancet.

Fetal sex.

J. Hamerton, 1970, Lancet.

An intersex goat with a bilaterally asymmetrical reproductive tract.

J. Hamerton, R. Short, S. Grieves, 1968, Journal of reproduction and fertility.

Down syndrome and recent demographic trends in Manitoba.

J. Hamerton, A. Hunter, J. Evans, 1978, Journal of medical genetics.

Characteristics of an HPRT-deficient chinese hamster cell line.

J. Hamerton, G. Douglas, P. A. Gee, 1974, Cytogenetics and cell genetics.

Abstracts of meeting presentations (Part 10 of 11)

R. L. Miller, D. Cox, K. Kidd, 1984 .

Human Population Cytogenetics

J. Hamerton, 1968 .

Prenatal diagnosis in Canada — 1990: A review

J. Hamerton, J. Evans, L. C. Stranc, 1994, Prenatal diagnosis.

Regional localization of loci for human PGM and 6PGD on human chromosome one by use of hybrids of Chinese hamster-human somatic cells.

J. Hamerton, G. Douglas, P. McAlpine, 1973, Proceedings of the National Academy of Sciences of the United States of America.

Tentative assignment of the peptidase-A (Pep-A) gene locus to the (q21 leads to qter) region of chromosome 18 in man.

T. Mohandas, J. Hamerton, P. McAlpine, 1975, Birth defects original article series.

Physical and psychologic parameters in children with sex chromosome anomalies: further follow-up from the Winnipeg Cytogenetic Study of 14,069 newborn infants.

J. Hamerton, C. Greenberg, J. Evans, 1986, Birth defects original article series.

Chapter 8 – ABNORMALITIES OF THE AUTOSOMES: TRISOMICS, DELETIONS, DUPLICATIONS, AND TRANSLOCATIONS (EXCEPT GROUPS D, E, AND G)

J. Hamerton, 1971 .

Deletion of the Long Arms of Chromosome 18 (46,XX,18q-) Associated with Absence of IgA and Hypothyroidism in an Adult

J. Hamerton, 2006 .

DETECTION AND CROSS‐REACTION OF H‐Y ANTIGEN BY HAEMAGGLUTINATION

J. Hamerton, I. Bérczi, A. Shalev, 1978, European journal of immunogenetics.

Banding patterns of metaphase chromosomes in Down's syndrome.

J. Hamerton, 1971, Lancet.

Abstracts of meeting presentations (Part 5 of 11)

A. Chapelle, J. Opitz, N. Morton, 1979 .

Collaborative studies in prenatal diagnosis of chromosome aberrations

J. Hamerton, 1984 .

Abstracts of meeting presentations (Part 11 of 11)

R. L. Miller, D. Cox, K. Kidd, 1984 .

A 48,XXXX female

J. Hamerton, G. Douglas, M. Ray, 1974, Journal of medical genetics.

Further data on the assignment of the phosphoglucomutase2 (PGM2) gene locus to chromosome 4 in man.

T. Mohandas, J. Hamerton, P. McAlpine, 1975, Cytogenetics and cell genetics.

The Chromosomes of Man

J. Hamerton, C. Ford, J. L. HAMERTON, 1956, Nature.

Report of the committee on the genetic constitution of chromosomes 1 and 2.

J. Hamerton, 1975, Birth defects original article series.

Paris Conference (1971): standardization in human cytogenetics.

J. Hamerton, 1972, Birth defects original article series.

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.

J. Hamerton, H. Wang, N. Christie, 1981, Cytogenetics and Cell Genetics.

The Chromosomes of the Hominoidea

J. Hamerton, H. Klinger, D. Mutton, 2017 .

Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man.

T. Mohandas, J. Hamerton, M. Ray, 1976, Birth defects original article series.

Demonstration of fluorescent X and Y bodies after antibody- and complement-mediated cytotoxicity

J. Hamerton, I. Bérczi, A. Shalev, 1977, Immunogenetics.

Physical and psychological findings in adolescents with sex chromosome abnormalities ascertained in the Winnipeg Cytogenetic Study of Newborns: 1970-1973.

J. Hamerton, C. Greenberg, J. Evans, 1990, Birth defects original article series.

Constitutive heterochromatin in mouse chromosomes treated with typsin.

J. Hamerton, M. Ray, 1973, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

SHORTENING OF LIFE IN THE OFFSPRING OF MALE MICE EXPOSED TO NEUTRON RADIATION FROM AN ATOMIC BOMB.

J. Hamerton, W. Russell, L. B. Russell, 1957, Proceedings of the National Academy of Sciences of the United States of America.