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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

Rare DiseasesFacioscapulohumeral Muscular DystrophyMendelian DisorderCorrect Genetic AdviceGenetic DisorderGeneticsMolecular BiologyReliable Prenatal DiagnosisDegenerative DiseaseMolecular GeneticsDisease Gene IdentificationMedicineClinical Genetics