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.
130 related articles for article (PubMed ID: 9673985)
1. 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]
2. Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p. Bashir R; Keers S; Strachan T; Passos-Bueno R; Zatz M; Weissenbach J; Le Paslier D; Meisler M; Bushby K Genomics; 1996 Apr; 33(1):46-52. PubMed ID: 8617508 [TBL] [Abstract][Full Text] [Related]
3. 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]
9. Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate region. Passos-Bueno MR; Bashir R; Moreira ES; Vainzof M; Marie SK; Vasquez L; Iughetti P; Bakker E; Keers S; Stephenson A Genomics; 1995 May; 27(1):192-5. PubMed ID: 7665169 [TBL] [Abstract][Full Text] [Related]
10. [Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13]. Illarioshkin SN; Ivanova-Smolenskaia IA; Dimborskaia SA; Poleshchuk VV; Markova ED; Slominskiĭ PA; Bulaeva KB; Tsudzi Sh Genetika; 1997 Nov; 33(11):1551-8. PubMed ID: 9480219 [TBL] [Abstract][Full Text] [Related]
11. The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12. Moreira ES; Vainzof M; Marie SK; Sertié AL; Zatz M; Passos-Bueno MR Am J Hum Genet; 1997 Jul; 61(1):151-9. PubMed ID: 9245996 [TBL] [Abstract][Full Text] [Related]
12. Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes. Bejaoui K; Liu J; McKenna-Yasek D; Le Paslier D; Bossie K; Gilligan DM; Brown RH Neurogenetics; 1998 Mar; 1(3):189-96. PubMed ID: 10737122 [TBL] [Abstract][Full Text] [Related]
13. Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy. Waggoner B; Kovach MJ; Winkelman M; Cai D; Khardori R; Gelber D; Kimonis VE Am J Med Genet; 2002 Mar; 108(3):187-91. PubMed ID: 11891683 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus. Weiler T; Greenberg CR; Zelinski T; Nylen E; Coghlan G; Crumley MJ; Fujiwara TM; Morgan K; Wrogemann K Am J Hum Genet; 1998 Jul; 63(1):140-7. PubMed ID: 9634523 [TBL] [Abstract][Full Text] [Related]
16. Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy. Speer MC; Gilchrist JM; Chutkow JG; McMichael R; Westbrook CA; Stajich JM; Jorgenson EM; Gaskell PC; Rosi BL; Ramesar R Am J Hum Genet; 1995 Dec; 57(6):1371-6. PubMed ID: 8533766 [TBL] [Abstract][Full Text] [Related]
17. Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q. Speer MC; Yamaoka LH; Gilchrist JH; Gaskell CP; Stajich JM; Vance JM; Kazantsev A; Lastra AA; Haynes CS; Beckmann JS Am J Hum Genet; 1992 Jun; 50(6):1211-7. PubMed ID: 1598902 [TBL] [Abstract][Full Text] [Related]
18. Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus. Allamand V; Broux O; Bourg N; Richard I; Tischfield JA; Hodes ME; Conneally PM; Fardeau M; Jackson CE; Beckmann JS Hum Mol Genet; 1995 Mar; 4(3):459-63. PubMed ID: 7795603 [TBL] [Abstract][Full Text] [Related]
19. Genetic linkage of Welander distal myopathy to chromosome 2p13. Ahlberg G; von Tell D; Borg K; Edström L; Anvret M Ann Neurol; 1999 Sep; 46(3):399-404. PubMed ID: 10482271 [TBL] [Abstract][Full Text] [Related]
20. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. Bueno MR; Moreira ES; Vainzof M; Chamberlain J; Marie SK; Pereira L; Akiyama J; Roberds SL; Campbell KP; Zatz M Hum Mol Genet; 1995 Jul; 4(7):1163-7. PubMed ID: 8528203 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]