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3. Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD). Lee JH; Goto K; Sahashi K; Nonaka I; Matsuda C; Arahata K Muscle Nerve Suppl; 1995; 2():S27-31. PubMed ID: 7739622 [TBL] [Abstract][Full Text] [Related]
4. Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35. Wijmenga C; Dauwerse HG; Padberg GW; Meyer N; Murray JC; Mills K; van Ommen GB; Hofker MH; Frants RR Muscle Nerve Suppl; 1995; 2():S14-8. PubMed ID: 7739620 [TBL] [Abstract][Full Text] [Related]
5. Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35. Lee JH; Goto K; Matsuda C; Arahata K Muscle Nerve Suppl; 1995; 2():S6-13. PubMed ID: 7739628 [TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
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. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q. Mathews KD; Mills KA; Bailey HL; Schelper RL; Murray JC Muscle Nerve Suppl; 1995; 2():S98-102. PubMed ID: 7739634 [TBL] [Abstract][Full Text] [Related]
11. Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library. Upadhyaya M; Osborn M; Maynard J; Altherr M; Ikeda J; Harper PS Am J Med Genet; 1995 Jun; 60(3):244-51. PubMed ID: 7573180 [TBL] [Abstract][Full Text] [Related]
12. Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35. van Deutekom JC; Hofker MH; Romberg S; van Geel M; Rommens J; Wright TJ; Hewitt JE; Padberg GW; Wijmenga C; Frants RR Muscle Nerve Suppl; 1995; 2():S19-26. PubMed ID: 7739621 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy. Lunt PW; Jardine PE; Koch M; Maynard J; Osborn M; Williams M; Harper PS; Upadhyaya M Muscle Nerve Suppl; 1995; 2():S103-9. PubMed ID: 7739619 [TBL] [Abstract][Full Text] [Related]
17. Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35. van Deutekom JC; Lemmers RJ; Grewal PK; van Geel M; Romberg S; Dauwerse HG; Wright TJ; Padberg GW; Hofker MH; Hewitt JE; Frants RR Hum Mol Genet; 1996 May; 5(5):581-90. PubMed ID: 8733123 [TBL] [Abstract][Full Text] [Related]
18. Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses. Arahata K; Ishihara T; Fukunaga H; Orimo S; Lee JH; Goto K; Nonaka I Muscle Nerve Suppl; 1995; 2():S56-66. PubMed ID: 7739627 [TBL] [Abstract][Full Text] [Related]
19. The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes. Lyle R; Wright TJ; Clark LN; Hewitt JE Genomics; 1995 Aug; 28(3):389-97. PubMed ID: 7490072 [TBL] [Abstract][Full Text] [Related]
20. The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus. Wijmenga C; Winokur ST; Padberg GW; Skraastad MI; Altherr MR; Wasmuth JJ; Murray JC; Hofker MH; Frants RR Hum Genet; 1993 Sep; 92(2):198-203. PubMed ID: 8103757 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]