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https://doi.org/10.1136/jmg-2023-109832
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Cite Journal: Journal of Medical Genetics |  Publication Date: Oct 25, 2024 |
BackgroundFacioscapulohumeral muscular dystrophy 1 (FSHD1) is an autosomal dominant muscular disorder mainly caused by the contraction and hypomethylation of the D4Z4 repeat array in chromosome 4q35. Prenatal diagnosis of FSHD1...
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