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Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5999, pp. 1650 - 1653
Journal Article
Journal Article
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 12, pp. 1370 - 1374
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 12/2018
OBJECTIVETo assess the relation between age at onset and disease severity in facioscapulohumeral muscular dystrophy (FSHD). METHODSIn this prospective... 
Journal Article
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 12/2015, Volume 85, Issue 24, pp. 2147 - 2150
OBJECTIVE:To examine the relationship of clinical and genetic features of patients with facioscapulohumeral muscular dystrophy (FSHD) with 7–10 residual D4Z4... 
FSHD | DNA REARRANGEMENTS | CLINICAL NEUROLOGY | FEATURES | Repetitive Sequences, Nucleic Acid - genetics | Prospective Studies | Cross-Sectional Studies | Muscular Dystrophy, Facioscapulohumeral - diagnosis | Humans | Middle Aged | Male | Muscular Dystrophy, Facioscapulohumeral - genetics | Young Adult | Phenotype | Adult | Female | Aged | 176 | 185
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 10/2018, Volume 27, Issue 20, pp. 3488 - 3497
Abstract Facioscapulohumeral muscular dystrophy, known in genetic forms FSHD1 and FSHD2, is associated with D4Z4 repeat array chromatin relaxation and somatic... 
PENETRANCE | SMCHD1 | METHYLATION | GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | SEQUENCE | GENETICS & HEREDITY | FSHD | DUX4 EXPRESSION | REARRANGEMENTS | LOCUS | 4Q
Journal Article
Journal Article