Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.-Reference-Cited by-同舟云学术

Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.

Published:1998-09-01 Issue:9 Volume:35 Page:778-783
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Tupler R,Barbierato L,Memmi M,Sewry C A,De Grandis D,Maraschio P,Tiepolo L,Ferlini A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference36 articles.

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3. Genetic counselling in facioscapulohumeral muscular dystrophy. 7Med Genet;Lunt, P.W.; Harper, P.S.,1992

4. Facioscapulohumeral muscular dystrophy: the choice of a biopsy site;Bodensteiner, J.B.; Schochet, S.S.;Muscle Nerve,1986

5. Muscle biopsies: a modern approach;Dubowitz, V.; Brooke, M.H.,1973

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