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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 9246005)

  • 1. DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene.
    Pratt VM; Jackson CE; Wallace DC; Gurley DS; Feit A; Feldman GL
    Am J Hum Genet; 1997 Jul; 61(1):231-3. PubMed ID: 9246005
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. An STS map of the limb girdle muscular dystrophy type 2A region.
    Richard I; Roudaut C; Fougerousse F; Chiannilkulchai N; Beckmann JS
    Mamm Genome; 1995 Oct; 6(10):754-6. PubMed ID: 8563179
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Lymphocyte capping in limb-girdle muscular dystrophy: patients and carriers in an Amish isolate.
    Bader PI; Bender CJ; Creason MT; Conn PS; Townsend DW
    Am J Med Genet; 1982 Jul; 12(3):255-69. PubMed ID: 7114089
    [No Abstract]   [Full Text] [Related]  

  • 8. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12.
    Lim LE; Duclos F; Broux O; Bourg N; Sunada Y; Allamand V; Meyer J; Richard I; Moomaw C; Slaughter C
    Nat Genet; 1995 Nov; 11(3):257-65. PubMed ID: 7581448
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Separation of dystrophinopathies from the group previously classified as limb-girdle muscular dystrophies].
    Kozłowska M; Bushby K; Bisko M; Zimowski J; Badurska B
    Neurol Neurochir Pol; 1994; 28(1 Suppl 1):115-24. PubMed ID: 8065538
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [Autosomal recessive limb-girdle muscular dystrophy probably linked to chromosome 15].
    Noguera Moya A; Lorenzo Sanz G; García Villanueva M; Benítez J; Aparicio Méix JM
    An Esp Pediatr; 1996 Mar; 44(3):267-9. PubMed ID: 8830604
    [No Abstract]   [Full Text] [Related]  

  • 12. A foundation for limb-girdle muscular dystrophy.
    van Ommen GJ
    Nat Med; 1995 May; 1(5):412-4. PubMed ID: 7585084
    [No Abstract]   [Full Text] [Related]  

  • 13. Limb girdle muscular dystrophy: reappraisal of a rejected entity.
    van der Kooi AJ; de Visser M; Barth PG
    Clin Neurol Neurosurg; 1994 Aug; 96(3):209-18. PubMed ID: 7988088
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular cloning of mouse canp3, the gene associated with limb-girdle muscular dystrophy 2A in human.
    Richard I; Beckmann JS
    Mamm Genome; 1996 May; 7(5):377-9. PubMed ID: 8661728
    [No Abstract]   [Full Text] [Related]  

  • 15. Cardiomyopathy of limb-girdle muscular dystrophy.
    Mascarenhas DA; Spodick DH; Chad DA; Gilchrist J; Townes PL; DeGirolami U; Mudge GH; Maki DW; Bishop RL
    J Am Coll Cardiol; 1994 Nov; 24(5):1328-33. PubMed ID: 7930257
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of limb-girdle muscular dystrophy type 2A.
    Restagno G; Romero N; Richard I; Beckmann JS; Pagliano M; Ferrone M; Carbonara A; Merlini L
    Neuromuscul Disord; 1996 May; 6(3):173-6. PubMed ID: 8784805
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies.
    Pogue R; Anderson LV; Pyle A; Sewry C; Pollitt C; Johnson MA; Davison K; Moss JA; Mercuri E; Muntoni F; Bushby KM
    Neuromuscul Disord; 2001 Jan; 11(1):80-7. PubMed ID: 11166169
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.
    Duclos F; Broux O; Bourg N; Straub V; Feldman GL; Sunada Y; Lim LE; Piccolo F; Cutshall S; Gary F; Quetier F; Kaplan JC; Jackson CE; Beckmann JS; Campbell KP
    Neuromuscul Disord; 1998 Feb; 8(1):30-8. PubMed ID: 9565988
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Understanding the heterogeneity of the limb-girdle muscular dystrophies.
    Bushby K
    Biochem Soc Trans; 1996 May; 24(2):489-96. PubMed ID: 8736790
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.