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Defining the chromosomal basis of mental handicap

The Lancet (British edition), 1999-11, Vol.354 (9191), p.1659-1660

1999

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Chorionic villus sampling and amniocentesis for prenatal diagnosis

The Lancet (British edition), 1997-03, Vol.349 (9053), p.711-714

1997

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Limb defects and chorionic villus sampling

The Lancet (British edition), 1996-02, Vol.347 (9000), p.484-485

1996

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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

Human genetics, 1991-11, Vol.88 (1), p.42-48

1991

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

Genomics (San Diego, Calif.), 1991-03, Vol.9 (3), p.524-535

1991

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

Canadian Medical Association journal, 1976-10, Vol.115 (8), p.739-748

1976

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

Somatic cell and molecular genetics, 1987-05, Vol.13 (3), p.285-292

1987

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Prenatal diagnosis in Canada - 1990: A review

Prenatal diagnosis, 1994-12, Vol.14 (13), p.1253-1265

1994

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Significance of Sex Chromosome Derived Heterochromatin in Mammals

Nature (London), 1968-08, Vol.219 (5157), p.910-914

HAMERTON, J. L

1968

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Isolation and characterization of a processed gene for human ceruloplasmin

Biochemistry (Easton), 1987-12, Vol.26 (24), p.7760-7767

1987

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A DNA marker for human chromosome 8 that detects alleles of differing sizes

Cytogenetic and genome research, 1986-01, Vol.42 (3), p.113-118

1986

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

Chromosoma, 1986-01, Vol.94 (3), p.228-234

1986

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

American journal of human genetics, 1987-08, Vol.41 (2), p.128-137

1987

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Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

Nature (London), 1986-07, Vol.322 (6074), p.73-77

Kunkel, Louis M

1986

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Regional localization of 18 human X-linked DNA sequences

Cytogenetic and genome research, 1986-01, Vol.42 (3), p.123-128

1986

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

Nature (London), 1982-08, Vol.298 (5874), p.563-565

1982

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56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy site

Nature (London), 1983-08, Vol.304 (5928), p.740-741

1983

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

American journal of medical genetics, 1991-09, Vol.40 (4), p.454-459

1991

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Two RFLPs identified by an anonymous sequence (D7S19) (pTS119) from chromosome 7

Nucleic acids research, 1987-03, Vol.15 (6), p.2784-2784

1987

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Human population cytogenetics: dilemmas and problems

American journal of human genetics, 1976-03, Vol.28 (2), p.107-122

Hamerton, J L

1976

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The gene for clotting factor 10 is mapped to 13q32----qter

Cytogenetic and genome research, 1986-01, Vol.41 (3), p.185-188

1986

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TaqI and RsaI RFLP's at the prolactin inducible protein (PIP) locus on chromosome 7

Nucleic acids research, 1989-07, Vol.17 (14), p.5879-5879

1989

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Report of the Committee on the Genetic Constitution of Chromosome 1

Cytogenetic and genome research, 1984-01, Vol.37 (1-4), p.3-21

1984

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

Somatic cell and molecular genetics, 1989-05, Vol.15 (3), p.265-270

1989

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

Somatic cell and molecular genetics, 1985-03, Vol.11 (2), p.189-195

1985

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Defining the chromosomal basis of mental handicap

Chorionic villus sampling and amniocentesis for prenatal diagnosis

Limb defects and chorionic villus sampling

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

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

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

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

Prenatal diagnosis in Canada - 1990: A review

Significance of Sex Chromosome Derived Heterochromatin in Mammals

Isolation and characterization of a processed gene for human ceruloplasmin

A DNA marker for human chromosome 8 that detects alleles of differing sizes

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

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

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

Regional localization of 18 human X-linked DNA sequences

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

56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy site

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

Two RFLPs identified by an anonymous sequence (D7S19) (pTS119) from chromosome 7

Human population cytogenetics: dilemmas and problems

The gene for clotting factor 10 is mapped to 13q32----qter

TaqI and RsaI RFLP's at the prolactin inducible protein (PIP) locus on chromosome 7

Report of the Committee on the Genetic Constitution of Chromosome 1

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

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

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