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3. Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD). Upadhyaya M; Maynard J; Osborn M; Jardine P; Harper PS; Lunt P Muscle Nerve Suppl; 1995; 2():S45-9. PubMed ID: 7739625 [TBL] [Abstract][Full Text] [Related]
4. Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD). Lunt PW; Jardine PE; Koch MC; Maynard J; Osborn M; Williams M; Harper PS; Upadhyaya M Hum Mol Genet; 1995 May; 4(5):951-8. PubMed ID: 7633457 [TBL] [Abstract][Full Text] [Related]
5. No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markers. Passos-Bueno MR; Wijmenga C; Takata RE; Marie SK; Vainzof M; Pavanello RC; Hewitt JE; Bakker E; Carvalho A; Akiyama J Hum Mol Genet; 1993 May; 2(5):557-62. PubMed ID: 8518794 [TBL] [Abstract][Full Text] [Related]
6. Detection of the mutation in facioscapulohumeral muscular dystrophy patients. Ohya K; Tachi N; Kozuka N; Kon S; Kikuchi K; Chiba S Acta Paediatr Jpn; 1997 Feb; 39(1):92-6. PubMed ID: 9124063 [TBL] [Abstract][Full Text] [Related]
7. Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions. Wijmenga C; van Deutekom JC; Hewitt JE; Padberg GW; van Ommen GJ; Hofker MH; Frants RR Genomics; 1994 Jan; 19(1):21-6. PubMed ID: 7910579 [TBL] [Abstract][Full Text] [Related]
8. Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression. Tupler R; Barbierato L; Memmi M; Sewry CA; De Grandis D; Maraschio P; Tiepolo L; Ferlini A J Med Genet; 1998 Sep; 35(9):778-83. PubMed ID: 9733041 [TBL] [Abstract][Full Text] [Related]
9. [Facioscapulohumeral muscular dystrophy (FSHD)]. Funakoshi M; Goto K; Kim BY; Arahata K Nihon Rinsho; 1997 Dec; 55(12):3181-5. PubMed ID: 9436432 [TBL] [Abstract][Full Text] [Related]
10. Germline mosaicism in 4q35 facioscapulohumeral muscular dystrophy (FSHD1A) occurring predominantly in oogenesis. Köhler J; Rupilius B; Otto M; Bathke K; Koch MC Hum Genet; 1996 Oct; 98(4):485-90. PubMed ID: 8792827 [TBL] [Abstract][Full Text] [Related]
11. A pediatric case report and literature review of facioscapulohumeral muscular dystrophy type1. Xiao T; Yang H; Gan S; Wu L Medicine (Baltimore); 2021 Nov; 100(47):e27907. PubMed ID: 34964760 [TBL] [Abstract][Full Text] [Related]
12. Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD). Upadhyaya M; Maynard J; Osborn M; Jardine P; Harper PS; Lunt P Muscle Nerve Suppl; 1995; (2):S45-9. PubMed ID: 23573586 [TBL] [Abstract][Full Text] [Related]