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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]
4. [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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
11. A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3. Driss A; Amouri R; Ben Hamida C; Souilem S; Gouider-Khouja N; Ben Hamida M; Hentati F Neuromuscul Disord; 2000 Jun; 10(4-5):240-6. PubMed ID: 10838249 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families. Passos-Bueno MR; Moreira ES; Marie SK; Bashir R; Vasquez L; Love DR; Vainzof M; Iughetti P; Oliveira JR; Bakker E; Strachan T; Bushby K; Zatz M J Med Genet; 1996 Feb; 33(2):97-102. PubMed ID: 8929943 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15. Velinov M; Sarfarazi M; Young K; Hodes ME; Conneally PM; Jackson CE; Tsipouras P Connect Tissue Res; 1993; 29(1):13-21. PubMed ID: 8339542 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence. Passos-Bueno MR; Terwilliger J; Ott J; Vainzof M; Love DR; Davies KE; Zatz M Am J Med Genet; 1991 Jan; 38(1):140-6. PubMed ID: 2012126 [TBL] [Abstract][Full Text] [Related]
20. Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD. Passos-Bueno MR; Moreira ES; Vainzof M; Marie SK; Zatz M Hum Mol Genet; 1996 Jun; 5(6):815-20. PubMed ID: 8776597 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]