Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere-Reference-Cited by-同舟云学术

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Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere

Published:2002-09-23 Issue:2 Volume:32 Page:235-236
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Lemmers Richard J.L.F.,de Kievit Peggy,Sandkuijl Lodewijk,Padberg George W.,van Ommen Gert-Jan B.,Frants Rune R.,van der Maarel Silvère M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng999z.pdf

Reference12 articles.

1. van Geel, M. et al. Genomics 79, 210–217 (2002).

2. Wijmenga, C. et al. Nature Genet. 2, 26–30 (1992).

3. van Overveld, P.G. et al. Hum. Mol. Genet. 9, 2879–2884 (2000).

4. van Deutekom, J.C.T. et al. Hum. Mol. Genet. 5, 581–590 (1996).

5. van Geel, M. et al. Cytogenet. Cell Genet. 88, 316–321 (2000).

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