Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy von Ray, Peter N, Belfall, Bonnie, Duff, Catherine, Logan, Cairine, Kean, Vanora, Thompson, Margaret W, Sylvester, James E, Gorski, Jerome L, Schmickel, Roy D, Worton, Ronald G

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A Functional Probe of Ligand Binding and Agonist Efficacy in Ionotropic Glutamate Receptors von Thompson, Margaret W., McMenimen, Kathryn A., Lester, Henry A., Dougherty, Dennis A.

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Analysis of effects of W and f genic substitutions on fetal mouse hematology von Russel, E S, Thompson, M W, McFarland, E

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The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease von Thompson, Margaret W.

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Genetics of Duchenne Muscular Dystrophy von Worton, R G, Thompson, M W

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Finger Pattern Combinations in Normal Individuals and in Down's Syndrome von Thompson, Margaret W., Bandler, Elizabeth

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Birthweight in Congenital Virilizing Adrenal Hyperplasia von Qazi, Qutub H., Thompson, Margaret W.

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Specific cellular defects in patients with Fanconi anemia von Weksberg, Rosanna, Buchwald, Manuel, Sargent, Patricia, Thompson, Margaret W., Siminovitch, Louis

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Genetics in Medicine von Thompson, James S., Thompson, Margaret W., Wilson, William G.

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Genetics in Medicine von Thompson, James S., Thompson, Margaret W., Wilson, William G.

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Clinical Review : Genetic Counseling in Clinical Pediatrics: What to Do with Inquiries about Heritable Disorders von Thompson, Margaret W.

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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... von Thompson, Margaret W.

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CARRIER DETECTION IN MUSCULAR DYSTROPHY von Thompson, MargaretW

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Genethics: Technological intervention in human reproduction as a philosophical problem von Thompson, Margaret W.

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Color atlas of genetics von Thompson, Margaret W.

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Book ReviewGenetics of Epilepsy: A review von Thompson, Margaret W.

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Book Review von Thompson, Margaret W

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Book Review von Thompson, Margaret W

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

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Serum creatine kinase in the detection of duchenne muscular dystrophy carriers: Effects of season and multiple testing von Percy, Maire E., Andrews, David F., Thompson, Margaret W.

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