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Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndrome
by
Renard, Dimitri
,
Taieb, Guillaume
,
Garibaldi, Matteo
,
Maues De Paula, Andre
,
Bernard, Rafaelle
,
Lagha, Nadira
,
Cristofari, Gael
,
Vovan, Catherine
,
Chaix, Charlène
,
Lévy, Nicolas
,
Khau Van Kien, Philippe
,
Sacconi, Sabrina
Published in
American journal of medical genetics. Part A
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American Journal Of Medical Genetics. Part A
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Subjects
18P Deletion Syndrome
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Chromatin
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Chromosome 18
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Chromosome 4
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Contraction
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Derepression
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Facioscapulohumeral Muscular Dystrophy Type 2
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Gene Mapping
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Genetics & Heredity
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Human Health And Pathology
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Hypomethylation
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Inflammation
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Inflammatory
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Life Sciences
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Life Sciences & Biomedicine
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Mri
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Muscle Biopsy
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Muscular Dystrophy
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Polyadenylation
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Rhumatology And Musculoskeletal System
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Wiley-Blackwell Journals
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Wiley
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