Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy-Reference-Cited by-同舟云学术

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Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy

Published:2001-09 Issue:6-7 Volume:11 Page:525-529
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Flanigan Kevin M,Coffeen Christin M,Sexton Lee,Stauffer Dora,Brunner Shari,Leppert Mark F

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference16 articles.

1. Facioscapulohumeral disease;Padberg,1982

2. Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH Consortium;Tawil;Ann Neurol,1998

3. Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element;Gabriels;Gene,1999

4. Position effects on eukaryotic gene expression;Wilson;Annu Rev Cell Biol,1990

5. Heterochromatin and gene expression in Drosophila;Weiler;Annu Rev Genet,1995

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