A clinically homogeneous group of families with facioscapulohumeral (Landouzy-déjérine) muscular dystrophy: Linkage analysis of six autosomes

Facioscapulohumeral muscular dystrophy (FSHMD) is a neuromuscular disorder characterized by autosomal dominant inheritance and clinical onset in the muscles of the face and shoulder girdle. Using a set of RFLP markers spaced at approximately 20 centimorgans, we have begun a systematic search for mar...

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Main Authors: Jacobsen, Stephen J., Diala, Edward S., Dorsey, Bruce V., Rising, Marcia B., Graveline, Rebecca, Falls, Kathleen, Schultz, Paul, Hogan, Christopher, Rediker, Kenneth, D'Amico, Colette, Weiffenbach, Barbara
Formato: Artigo
Idioma:Inglês
Publicado em: 1990
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683887/
https://ncbi.nlm.nih.gov/pubmed/1975474
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