Facioscapulohumeral Dystrophy-Reference-Cited by-同舟云学术

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Facioscapulohumeral Dystrophy

Published:2015 Issue: Volume: Page:620-630
ISSN:
Container-title:Neuromuscular Disorders of Infancy, Childhood, and Adolescence
language:
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Author:

Liew Wendy K.M.,van der Maarel Silvère M.,Tawil Rabi

Publisher

Elsevier

Reference89 articles.

1. Facioscapulohumeral muscular dystrophy in the Dutch population;Padberg;Muscle Nerve Suppl,1995

2. De la myopathie atrophique progressive (myopathie héréditaire, débutant dans l’enfance par la face, sans altération du systéme nerveux);Landouzy;C R Acad Sci Gen (Paris),1884

3. Studies in disorders of muscle. II. Clinical manifestations and inheritance of facioscapulohumeral dystrophy in a large family;Tyler;Ann Intern Med,1950

4. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2kb tandemly repeated unit;van Deutekom;Hum Mol Genet,1993

5. 44th ENMC International Workshop: Facioscapulohumeral Muscular Dystrophy: Molecular Studies. 19–21 July 1996, Naarden, The Netherlands;Lunt;Neuromuscul Disord,1998

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