Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitness.

Author:

Eggers S,Passos-Bueno M R,Zatz M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. Genetic counselling in facioscapulohumeral muscular dystrophy;Lunt, P.W.; Harper, P.S.;7 Med Genet,1991

2. Facioscapulohumeral disease;Padberg, G.,1982

3. Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias;Lunt, P.W.; Compston, D.A.S.; Harper, P.S.;7 Med Genet,1989

4. Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage and in situ hybridization;Wijmenga, C.; Padberg, G.W.; Moerer, P.;Genomics,1992

5. Feasibility of newborn screening for Duchenne muscular dystrophy..7 Med;Skinner, R.; Emery, A.E.H.; Scheuerbrandt, G.; Syme, J.;Genet,1982

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1. The facioscapulohumeral muscular dystrophy – health index: Italian validation of a disease-specific measure of symptomatic burden;Disability and Rehabilitation;2023-05-17

2. Facioscapulohumeral Muscular Dystrophy;Atlas of Genetic Diagnosis and Counseling;2017

3. Facioscapulohumeral Muscular Dystrophy;Atlas of Genetic Diagnosis and Counseling;2015

4. Facioscapulohumeral Muscular Dystrophy;Atlas of Genetic Diagnosis and Counseling;2012

5. Neuromuscular rehabilitation and electrodiagnosis. 5. Myopathy;Archives of Physical Medicine and Rehabilitation;2000-03

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