These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Molecular diagnosis of facioscapulohumeral muscular dystrophy. Upadhyaya M; Cooper DN Expert Rev Mol Diagn; 2002 Mar; 2(2):160-71. PubMed ID: 11962336 [TBL] [Abstract][Full Text] [Related]
6. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q. Jiang G; Yang F; van Overveld PG; Vedanarayanan V; van der Maarel S; Ehrlich M Hum Mol Genet; 2003 Nov; 12(22):2909-21. PubMed ID: 14506132 [TBL] [Abstract][Full Text] [Related]
7. Facioscapulohumeral muscular dystrophy. Tawil R; Van Der Maarel SM Muscle Nerve; 2006 Jul; 34(1):1-15. PubMed ID: 16508966 [TBL] [Abstract][Full Text] [Related]
8. Characterization of a tandemly repeated 3.3-kb Kpnl 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: 23573580 [TBL] [Abstract][Full Text] [Related]
9. The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease. Winokur ST; Bengtsson U; Feddersen J; Mathews KD; Weiffenbach B; Bailey H; Markovich RP; Murray JC; Wasmuth JJ; Altherr MR Chromosome Res; 1994 May; 2(3):225-34. PubMed ID: 8069466 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
15. 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]
16. Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion. Krasnianski M; Eger K; Neudecker S; Jakubiczka S; Zierz S Arch Neurol; 2003 Oct; 60(10):1421-5. PubMed ID: 14568813 [TBL] [Abstract][Full Text] [Related]
17. Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Winokur ST; Chen YW; Masny PS; Martin JH; Ehmsen JT; Tapscott SJ; van der Maarel SM; Hayashi Y; Flanigan KM Hum Mol Genet; 2003 Nov; 12(22):2895-907. PubMed ID: 14519683 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Translocation between chromosomes 4q35 and 10q26 in facioscapulohumeral muscular dystrophy]. Su QX; Zhang C; Zeng Y; Lu XL; Liu XR; Wang ZH; Zhu YZ Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Oct; 25(5):581-4. PubMed ID: 14650163 [TBL] [Abstract][Full Text] [Related]
20. [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] [Next] [New Search]