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6. Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD). Cacurri S; Deidda G; Piazzo N; Novelletto A; La Cesa I; Servidei S; Galluzzi G; Wijmenga C; Frants RR; Felicetti L Hum Genet; 1994 Oct; 94(4):367-74. PubMed ID: 7927331 [TBL] [Abstract][Full Text] [Related]
7. [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]
8. 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]
9. 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]
10. Molecular genetics of facioscapulohumeral muscular dystrophy. Wijmenga C; Frants RR; Hewitt JE; van Deutekom JC; van Geel M; Wright TJ; Padberg GW; Hofker MH; van Ommen GJ Neuromuscul Disord; 1993; 3(5-6):487-91. PubMed ID: 8186699 [TBL] [Abstract][Full Text] [Related]
11. The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter. Bakker E; Wijmenga C; Vossen RH; Padberg GW; Hewitt J; van der Wielen M; Rasmussen K; Frants RR Muscle Nerve Suppl; 1995; 2():S39-44. PubMed ID: 7739624 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter. Deidda G; Cacurri S; Grisanti P; Vigneti E; Piazzo N; Felicetti L Eur J Hum Genet; 1995; 3(3):155-67. PubMed ID: 7583041 [TBL] [Abstract][Full Text] [Related]
15. Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD). Lee JH; Goto K; Sahashi KO; Nonaka I; Matsuda C; Arahata K Muscle Nerve Suppl; 1995; (2):S27-31. PubMed ID: 23573583 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter. Bakker E; Wijmenga C; Vossen RH; Padberg GW; Hewitt J; van der Wielen M; Rasmussen K; Frants RR Muscle Nerve Suppl; 1995; (2):S39-44. PubMed ID: 23573585 [TBL] [Abstract][Full Text] [Related]
18. [Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)]. Goto K; Song MD; Lee JH; Arahata K Rinsho Shinkeigaku; 1995 Dec; 35(12):1416-8. PubMed ID: 8752415 [TBL] [Abstract][Full Text] [Related]
20. An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD). Busse K; Köhler J; Stegmann K; Pongratz D; Koch MC; Schreiber H Neuromuscul Disord; 2000 Mar; 10(3):178-81. PubMed ID: 10734264 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]