Genetics of Facioscapulohumeral Muscular Dystrophy
More than 500 subjects from 41 families with dominantly inherited facioscapulohumeral muscular dystrophy (FSHD) were studied at the Royal Hospital for Sick Children, St. Michael’s Hill, Bristol and the University of Wales College of Medicine, Heath Park, Cardiff, Wales.
Saved in:
| Main Author: | J Gordon Millichap |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Pediatric Neurology Briefs Publishers
1991-11-01
|
| Series: | Pediatric Neurology Briefs |
| Subjects: | |
| Online Access: | https://www.pediatricneurologybriefs.com/articles/3137 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Case report of a child with combined genetic pathology: cystic fibrosis and facioscapulohumeral progressive muscular dystrophy
by: O. A. Klochkova, et al.
Published: (2015-02-01) -
Therapeutic Strategy and Clinical Path of Facioscapulohumeral Muscular Dystrophy: Review of the Current Literature
by: Qi Xie, et al.
Published: (2024-09-01) -
Speech and swallowing characteristics in patients with facioscapulohumeral muscular dystrophy
by: Vanessa Brzoskowski dos SANTOS, et al.
Published: (2022-02-01) -
Facioscapulohumeral muscular dystrophy: a review of pathogenesis, clinical symptoms, and treatment
by: T. Mikalauskas, et al.
Published: (2023-10-01) -
Quantitative Three-dimensional Scanning of Facial Movements in Facioscapulohumeral Dystrophy
by: Ceren Hangul, et al.
Published: (2025-04-01)