Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

Author:

Davies K E,Smith T J,Bundey S,Read A P,Flint T,Bell M,Speer A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference13 articles.

1. Phenotypic manifestations of X- autosome translocations;Elejalde, B.R.; Elejalde, M.M.,1983

2. Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy. Clin Genet determined;Boyd, Y.; Buckle, V.J.,1986

3. Cloning of the breakpoint of an X; 21 translocation associated with Duchenne muscular dystrophy;Ray, P.N.; Belfall, B.; Duff, C.;Nature,1985

4. Molecular analysis of the Duchenne muscular dystrophy region using pulsed-field gel electrophoresis;Kenwrick, S.; Patterson, M.N.; Speer, A.;Cell,1987

5. Long range restriction map around the Duchenne muscular dystrophy gene using pulsed-field gel electrophoresis;Burmeister, M.; Lehrach, H.;Nature,1986

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