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22. Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7. Speer MC; Vance JM; Grubber JM; Lennon Graham F; Stajich JM; Viles KD; Rogala A; McMichael R; Chutkow J; Goldsmith C; Tim RW; Pericak-Vance MA Am J Hum Genet; 1999 Feb; 64(2):556-62. PubMed ID: 9973293 [TBL] [Abstract][Full Text] [Related]
23. Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9). Fadda S; Mochi M; Roncuzzi L; Sangiorgi S; Sbarra D; Zatz M; Romeo G Hum Genet; 1985; 71(1):33-6. PubMed ID: 2993155 [TBL] [Abstract][Full Text] [Related]
24. Assignment of the tibial muscular dystrophy locus to chromosome 2q31. Haravuori H; Mäkelä-Bengs P; Udd B; Partanen J; Pulkkinen L; Somer H; Peltonen L Am J Hum Genet; 1998 Mar; 62(3):620-6. PubMed ID: 9497249 [TBL] [Abstract][Full Text] [Related]
25. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Ben Othmane K; Ben Hamida M; Pericak-Vance MA; Ben Hamida C; Blel S; Carter SC; Bowcock AM; Petruhkin K; Gilliam TC; Roses AD Nat Genet; 1992 Dec; 2(4):315-7. PubMed ID: 1303286 [TBL] [Abstract][Full Text] [Related]
26. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Bejaoui K; Hirabayashi K; Hentati F; Haines JL; Ben Hamida C; Belal S; Miller RG; McKenna-Yasek D; Weissenbach J; Rowland LP Neurology; 1995 Apr; 45(4):768-72. PubMed ID: 7723968 [TBL] [Abstract][Full Text] [Related]
27. Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy. Wilcox DE; Affara NA; Yates JR; Ferguson-Smith MA; Pearson PL Hum Genet; 1985; 70(4):365-75. PubMed ID: 3860471 [TBL] [Abstract][Full Text] [Related]
28. A clinically homogeneous group of families with facioscapulohumeral (Landouzy-Déjérine) muscular dystrophy: linkage analysis of six autosomes. Jacobsen SJ; Diala ES; Dorsey BV; Rising MB; Graveline R; Falls K; Schultz P; Hogan C; Rediker K; D'Amico C Am J Hum Genet; 1990 Sep; 47(3):376-88. PubMed ID: 1975474 [TBL] [Abstract][Full Text] [Related]
29. Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28. Yates JR; Warner JP; Smith JA; Deymeer F; Azulay JP; Hausmanowa-Petrusewicz I; Zaremba J; Borkowska J; Affara NA; Ferguson-Smith MA J Med Genet; 1993 Feb; 30(2):108-11. PubMed ID: 8445613 [TBL] [Abstract][Full Text] [Related]
30. Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium. Toda T; Ikegawa S; Okui K; Kondo E; Saito K; Fukuyama Y; Yoshioka M; Kumagai T; Suzumori K; Kanazawa I Am J Hum Genet; 1994 Nov; 55(5):946-50. PubMed ID: 7977357 [TBL] [Abstract][Full Text] [Related]
31. Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipation. Gamez J; Navarro C; Andreu AL; Fernandez JM; Palenzuela L; Tejeira S; Fernandez-Hojas R; Schwartz S; Karadimas C; DiMauro S; Hirano M; Cervera C Neurology; 2001 Feb; 56(4):450-4. PubMed ID: 11222786 [TBL] [Abstract][Full Text] [Related]
32. Genetic heterogeneity in Miyoshi-type distal muscular dystrophy. Linssen WH; de Visser M; Notermans NC; Vreyling JP; Van Doorn PA; Wokke JH; Baas F; Bolhuis PA Neuromuscul Disord; 1998 Jun; 8(5):317-20. PubMed ID: 9673985 [TBL] [Abstract][Full Text] [Related]
33. Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype. Weiler T; Greenberg CR; Nylen E; Halliday W; Morgan K; Eggertson D; Wrogemann K Am J Hum Genet; 1996 Oct; 59(4):872-8. PubMed ID: 8808603 [TBL] [Abstract][Full Text] [Related]
34. A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12. Jarry J; Rioux MF; Bolduc V; Robitaille Y; Khoury V; Thiffault I; Tétreault M; Loisel L; Bouchard JP; Brais B Brain; 2007 Feb; 130(Pt 2):368-80. PubMed ID: 17008331 [TBL] [Abstract][Full Text] [Related]
35. Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy. Brown CS; Thomas NS; Sarfarazi M; Davies KE; Kunkel L; Pearson PL; Kingston HM; Shaw DJ; Harper PS Hum Genet; 1985; 71(1):62-74. PubMed ID: 2993158 [TBL] [Abstract][Full Text] [Related]