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2. 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]
3. 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]
4. 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]
5. 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]
7. Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families. Passos-Bueno MR; Richard I; Vainzof M; Fougerousse F; Weissenbach J; Broux O; Cohen D; Akiyama J; Marie SK; Carvalho AA J Med Genet; 1993 May; 30(5):385-7. PubMed ID: 8320700 [TBL] [Abstract][Full Text] [Related]
8. Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy. Illarioshkin SN; Ivanova-Smolenskaya IA; Tanaka H; Vereshchagin NV; Markova ED; Poleshchuk VV; Lozhnikova SM; Sukhorukov VS; Limborska SA; Slominsky PA; Bulayeva KB; Tsuji S Brain; 1996 Dec; 119 ( Pt 6)():1895-909. PubMed ID: 9009996 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Limb-girdle muscular dystrophy: a follow-up study of 79 patients. Mahjneh I; Bushby K; Pizzi A; Bashir R; Marconi G Acta Neurol Scand; 1996 Sep; 94(3):177-89. PubMed ID: 8899051 [TBL] [Abstract][Full Text] [Related]
11. A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. Dinçer P; Leturcq F; Richard I; Piccolo F; Yalnizoglu D; de Toma C; Akçören Z; Broux O; Deburgrave N; Brenguier L; Roudaut C; Urtizberea JA; Jung D; Tan E; Jeanpierre M; Campbell KP; Kaplan JC; Beckmann JS; Topaloglu H Ann Neurol; 1997 Aug; 42(2):222-9. PubMed ID: 9266733 [TBL] [Abstract][Full Text] [Related]
12. The 10 autosomal recessive limb-girdle muscular dystrophies. Zatz M; de Paula F; Starling A; Vainzof M Neuromuscul Disord; 2003 Sep; 13(7-8):532-44. PubMed ID: 12921790 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy. Richard I; Broux O; Hillaire D; Cherif D; Fougerousse F; Cohen D; Beckmann JS Hum Mol Genet; 1992 Nov; 1(8):621-4. PubMed ID: 1363783 [TBL] [Abstract][Full Text] [Related]