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Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy

Nature (London), 1985-01, Vol.318 (6047), p.672-675

1985

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A Functional Probe of Ligand Binding and Agonist Efficacy in Ionotropic Glutamate Receptors

Biophysical journal, 2010-01, Vol.98 (3), p.526a-526a

2010

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Analysis of effects of W and f genic substitutions on fetal mouse hematology

Genetics (Austin), 1968-02, Vol.58 (2), p.259-270

1968

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The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease

Trends in genetics, 1996-03, Vol.12 (3), p.119

Thompson, Margaret W.

1996

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METHODOLOGY IN HUMAN GENETICS

Canadian journal of genetics and cytology, 1968-09, Vol.10 (3), p.747-753

Thompson, Margaret W.

1968

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Genetics of Duchenne Muscular Dystrophy

Annual review of genetics, 1988-01, Vol.22 (1), p.601-629

1988

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Finger Pattern Combinations in Normal Individuals and in Down's Syndrome

Human biology, 1973-12, Vol.45 (4), p.563-570

1973

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Delayed Implantation

Canadian journal of genetics and cytology, 1965, Vol.7 (1), p.175-175

Thompson, Margaret W.

1965

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21-trisomy in a fertile female mongol

Canadian journal of genetics and cytology, 1962-09, Vol.4 (3), p.352-355

THOMPSON, M W

1962

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Birthweight in Congenital Virilizing Adrenal Hyperplasia

Archives of disease in childhood, 1971-06, Vol.46 (247), p.350-352

1971

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GENETIC IMPLICATIONS OF HETEROPYKNOSIS OF THE X CHROMOSOME

Canadian journal of genetics and cytology, 1965-06, Vol.7 (2), p.202-213

THOMPSON, M W

1965

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Reproduction in two female mongols

Canadian journal of genetics and cytology, 1961-12, Vol.3 (4), p.351-354

THOMPSON, M W

1961

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Dermatoglyphics in congenital virilizing adrenal hyperplasia

American journal of diseases of children (1960), 1971-07, Vol.122 (1), p.28

1971

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Specific cellular defects in patients with Fanconi anemia

Journal of cellular physiology, 1979-11, Vol.101 (2), p.311-323

1979

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Genetics in Medicine

Journal of pediatric gastroenterology and nutrition, 1987-11, Vol.6 (6), p.1000-1000

1987

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Genetics in Medicine

Journal of pediatric gastroenterology and nutrition, 1987-11, Vol.6 (6), p.1000

1987

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Clinical Review : Genetic Counseling in Clinical Pediatrics: What to Do with Inquiries about Heritable Disorders

Clinical Pediatrics, 1967-04, Vol.6 (4), p.199-209

Thompson, Margaret W.

1967

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The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease: by Alan E.H. Emery and Marcia L.H. Emery Royal Society of Medicine Press, 1995. £20.00/$40.00 hbk (xvii and 248 pages) ISBN 1 85315 249 8

Trends in Genetics, 1996, Vol.12 (3), p.119-119

Thompson, Margaret W.

1996

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Heredity, maternal age, and birth order in the etiology of celiac disease1

American journal of human genetics, 1951-06, Vol.3 (2), p.159-166

Thompson, Margaret W.

1951

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CARRIER DETECTION IN MUSCULAR DYSTROPHY

The Lancet (British edition), 1962-11, Vol.280 (7265), p.1120-1121

Thompson, MargaretW

1962

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Color atlas of genetics

American Journal of Medical Genetics, 1996, Vol.66 (3), p.370-370

Thompson, Margaret W.

1996

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Genethics: Technological intervention in human reproduction as a philosophical problem

American Journal of Medical Genetics, 1996, Vol.66 (3), p.369-369

Thompson, Margaret W.

1996

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Book ReviewGenetics of Epilepsy: A review

New England Journal of Medicine, 1980, Vol.303 (13), p.763-764

Thompson, Margaret W.

1980

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Heritable disorders in orthopaedic practice. Ruth Wynne-Davies. Black-well, Oxford, 1973. 231 pp

Teratology, 1974, Vol.10 (2), p.209-210

Thompson, Margaret W.

1974

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Serum creatine kinase in the detection of duchenne muscular dystrophy carriers: Effects of season and multiple testing

Muscle & nerve, 1982-01, Vol.5 (1), p.58-64

1982

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Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy

A Functional Probe of Ligand Binding and Agonist Efficacy in Ionotropic Glutamate Receptors

Analysis of effects of W and f genic substitutions on fetal mouse hematology

The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease

METHODOLOGY IN HUMAN GENETICS

Genetics of Duchenne Muscular Dystrophy

Finger Pattern Combinations in Normal Individuals and in Down's Syndrome

Delayed Implantation

21-trisomy in a fertile female mongol

Birthweight in Congenital Virilizing Adrenal Hyperplasia

GENETIC IMPLICATIONS OF HETEROPYKNOSIS OF THE X CHROMOSOME

Reproduction in two female mongols

Dermatoglyphics in congenital virilizing adrenal hyperplasia

Specific cellular defects in patients with Fanconi anemia

Genetics in Medicine

Genetics in Medicine

Clinical Review : Genetic Counseling in Clinical Pediatrics: What to Do with Inquiries about Heritable Disorders

The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease: by Alan E.H. Emery and Marcia L.H. Emery Royal Society of Medicine Press, 1995. £20.00/$40.00 hbk (xvii and 248 pages) ISBN 1 85315 249 8

Heredity, maternal age, and birth order in the etiology of celiac disease1

CARRIER DETECTION IN MUSCULAR DYSTROPHY

Color atlas of genetics

Genethics: Technological intervention in human reproduction as a philosophical problem

Book ReviewGenetics of Epilepsy: A review

Heritable disorders in orthopaedic practice. Ruth Wynne-Davies. Black-well, Oxford, 1973. 231 pp

Serum creatine kinase in the detection of duchenne muscular dystrophy carriers: Effects of season and multiple testing

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