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Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease

✍ Scribed by G Galluzzi; G Deidda; S Cacurri; L Colantoni; N Piazzo; E Vigneti; E Ricci; S Servidei; B Merico; A Pachı̀; B Brambati; F Mangiola; P Tonali; L Felicetti


Book ID
118606697
Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
430 KB
Volume
9
Category
Article
ISSN
0960-8966

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