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9. The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD). Upadhyaya M; Lunt P; Sarfarazi M; Broadhead W; Farnham J; Harper PS Am J Hum Genet; 1992 Aug; 51(2):404-10. PubMed ID: 1642238 [TBL] [Abstract][Full Text] [Related]
10. Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region. Wijmenga C; Wright TJ; Baan MJ; Padberg GW; Williamson R; van Ommen GJ; Hewitt JE; Hofker MH; Frants RR Hum Mol Genet; 1993 Oct; 2(10):1667-72. PubMed ID: 8268920 [TBL] [Abstract][Full Text] [Related]
11. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy. Murray JM; Davies KE; Harper PS; Meredith L; Mueller CR; Williamson R Nature; 1982 Nov; 300(5887):69-71. PubMed ID: 6982420 [No Abstract] [Full Text] [Related]
12. Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD). Mills KA; Buetow KH; Xu Y; Ritty TM; Mathews KD; Bodrug SE; Wijmenga C; Balazs I; Murray JC Am J Hum Genet; 1992 Aug; 51(2):432-9. PubMed ID: 1642243 [TBL] [Abstract][Full Text] [Related]
14. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit. van Deutekom JC; Wijmenga C; van Tienhoven EA; Gruter AM; Hewitt JE; Padberg GW; van Ommen GJ; Hofker MH; Frants RR Hum Mol Genet; 1993 Dec; 2(12):2037-42. PubMed ID: 8111371 [TBL] [Abstract][Full Text] [Related]
15. [Gene hunting of facioscapulohumeral muscular dystrophy]. Song MD; Arahata K No To Shinkei; 1996 Apr; 48(4):307-13. PubMed ID: 8679326 [No Abstract] [Full Text] [Related]
18. A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy. Yaraghi Z; McLean MD; Roy N; Surh L; Ikeda JE; Korneluk RG; MacKenzie A Hum Genet; 1995 Sep; 96(3):330-4. PubMed ID: 7649551 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy. Cacurri S; Piazzo N; Deidda G; Vigneti E; Galluzzi G; Colantoni L; Merico B; Ricci E; Felicetti L Am J Hum Genet; 1998 Jul; 63(1):181-90. PubMed ID: 9634507 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]