Genetics of Facioscapulohumeral Dystrophy
The relationship of phenotype to genotype in a clinically and genetically well defined population of 157 affected patients and 62 kindreds with facioscapulohumeral muscular dystrophy (FSHD) was examined at the University of Rochester School of Medicine, NY, and Ohio State University, Columbus, OH.
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| Format: | Artigo |
| Idioma: | Inglês |
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Pediatric Neurology Briefs Publishers
1996-08-01
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| Col·lecció: | Pediatric Neurology Briefs |
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| Accés en línia: | https://www.pediatricneurologybriefs.com/articles/3776 |
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