Diagnostic criteria for facioscapulohumeral muscular dystrophy

Neuromuscular Disorders

Volumn 1, Issue 4, 1991, Pages 231-234

  Padberg, G W ^a   Lunt, P W ^b   Koch, M ^c   Fardeau, M ^d  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b BRISTOL ROYAL HOSPITAL FOR CHILDREN   (United Kingdom)

^c Institut für Humangenetikder Phillips Universität ^*  (Netherlands)

^d Institut National de la Santé et de la Recherche Médicale ^*  (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME; CHROMOSOME 4; CONFERENCE PAPER; FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; HUMAN;

FACIAL MUSCLES; HUMAN; HUMERUS; LINKAGE (GENETICS); MUSCULAR DYSTROPHIES; SCAPULA; SUPPORT, NON-U.S. GOV'T;

EID: 0026335673     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/0960-8966(91)90094-9     Document Type: Article

References (8)

1. The facioscapulohumeral muscular dystrophy gene maps to chromosome 4
2. DNA marker applicable to presymptomatic and prenatal diagnosis of Facioscapulohumeral disease
3. Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization
4. Revue Neurologique (Paris)
5. Facioscapulohumeral dystrophy and the scapulohumeral syndrome
6. Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias