PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

Author:

Bakker E,Goor N,Wrogemann K,Kunkel L.M,Fenton W.A,Majoor-Krakauer D,Jahoda M.G.J,Ommen G.J.B.Van,Hofker M.H,Mandel J.L,Davies K.E,Willard H.F,Sandkuyl L,Essen A.J.V,Sachs E.S,Pearson P.L

Publisher

Elsevier BV

Subject

General Medicine

Reference26 articles.

1. The biochemical identification of carrier state in X-linked (Duchenne) muscular dystrophy;Thomson;Clin Chim Acta,1969

2. Linkage relationship of a cloned DNA sequence on the short arm of X chromosome to Duchenne muscular dystrophy;Murray;Nature,1982

3. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of human X chromosome;Davies;Nucleic Acids Res,1983

4. Recombinant DNA techniques for mapping the human X chromosome;Bakker;Clin Genet,1983

5. C. Ingle, R. Williamson, A. de la Chapelle, et al., Mapping DNA sequences in a human X chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation, Am J Hum Genet ((in press)).

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