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Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

✍ Scribed by Mark Richards; Frédérique Coppée; Nick Thomas; Alexandra Belayew; Meena Upadhyaya


Book ID
106135220
Publisher
Springer
Year
2011
Tongue
English
Weight
980 KB
Volume
131
Category
Article
ISSN
0340-6717

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This study outlines the molecular DNA findings derived from 12 separate prenatal diagnoses offered to families with a history of facioscapulohumeral muscular dystrophy. A high risk of the fetus being affected was identified in five pregnancies. Several practical problems are discussed, particularly