BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 7795603)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.
    Allamand V; Broux O; Richard I; Fougerousse F; Chiannilkulchai N; Bourg N; Brenguier L; Devaud C; Pasturaud P; Pereira de Souza A
    Am J Hum Genet; 1995 Jun; 56(6):1417-30. PubMed ID: 7762565
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.
    Speer MC; Vance JM; Lennon-Graham F; Stajich JM; Viles KD; Gilchrist JM; Nigro V; McMichael R; Chutkow JG; Bartoloni L; Horrigan SK; Westbrook CA; Pericak-Vance MA
    Hum Hered; 1998; 48(4):179-84. PubMed ID: 9694248
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 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. Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.
    Young K; Foroud T; Williams P; Jackson CE; Beckmann JS; Cohen D; Conneally PM; Tischfield J; Hodes ME
    Genomics; 1992 Aug; 13(4):1370-1. PubMed ID: 1505977
    [No Abstract]   [Full Text] [Related]  

  • 17. Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene.
    Illarioshkin SN; Ivanova-Smolenskaya IA; Tanaka H; Poleshchuk VV; Markova ED; Tsuji S
    Genomics; 1997 Jun; 42(2):345-8. PubMed ID: 9192858
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.
    Richard I; Brenguier L; Dinçer P; Roudaut C; Bady B; Burgunder JM; Chemaly R; Garcia CA; Halaby G; Jackson CE; Kurnit DM; Lefranc G; Legum C; Loiselet J; Merlini L; Nivelon-Chevallier A; Ollagnon-Roman E; Restagno G; Topaloglu H; Beckmann JS
    Am J Hum Genet; 1997 May; 60(5):1128-38. PubMed ID: 9150160
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.