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Article

Germline mosaicism in 4q35 facioscapulohumeral muscular dystrophy (FSHD1A) occurring predominantly in oogenesis

22 Aug 1996

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 8792827
DOI: 10.1007/s004390050244

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Source receipt: pubmed, retrieved 7 Sept 2026.

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Germline mosaicism in 4q35 facioscapulohumeral muscular dystrophy (FSHD1A) occurring predominantly in oogenesisPMID 8792827Read ↗

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Clinical and genetic features of somatic mosaicism in facioscapulohumeral dystrophy.Semantic proximity Read ↗

Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophy.Semantic proximity Read ↗

Clinical and histopathological heterogeneity in patients with 4q35 facioscapulohumeral muscular dystrophy (FSHD).Semantic proximity Read ↗

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Everything, everywhere: FSHD as a model for complex genetic diseaseSemantic proximity Read ↗

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De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.Semantic proximity Read ↗

Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families.Semantic proximity Read ↗

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