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Journal Abstract Search

192 related items for PubMed ID: 8818946

  • 1. Linkage disequilibrium between four intragenic polymorphic microsatellites of the NF1 gene and its implications for genetic counselling.
    Valero MC, Velasco E, Valero A, Moreno F, Hernández-Chico C.
    J Med Genet; 1996 Jul; 33(7):590-3. PubMed ID: 8818946
    [Abstract] [Full Text] [Related]

  • 2. Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec population.
    Fang LJ, Li W, Chalhoub N, Feingold J, Ortenberg J, Thirion JP.
    Ann Genet; 2002 Jul; 45(1):39-44. PubMed ID: 11934389
    [Abstract] [Full Text] [Related]

  • 3. Genotype analysis of the NF1 gene in the French Canadians from the Québec population.
    Fang L, Chalhoub N, Li W, Feingold J, Ortenberg J, Lemieux B, Thirion JP.
    Am J Med Genet; 2001 Dec 01; 104(3):189-98. PubMed ID: 11754043
    [Abstract] [Full Text] [Related]

  • 4. Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population.
    Natacci F, Colapietro P, Riva P, Corrado L, Rossi LN, Maninetti MM, Casciati MC, Zambrino Ca, Lanzi G, Larizza L.
    Mol Cell Probes; 1999 Dec 01; 13(6):415-20. PubMed ID: 10657145
    [Abstract] [Full Text] [Related]

  • 5. Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) gene.
    Lázaro C, Gaona A, Ravella A, Volpini V, Casals T, Fuentes JJ, Estivill X.
    Hum Mol Genet; 1993 Jun 01; 2(6):725-30. PubMed ID: 8353492
    [Abstract] [Full Text] [Related]

  • 6. Genotyping of PCR-based polymorphisms and linkage-disequilibrium analysis at the NF1 locus.
    Purandare SM, Cawthon R, Nelson LM, Sawada S, Watkins WS, Ward K, Jorde LB, Viskochil DH.
    Am J Hum Genet; 1996 Jul 01; 59(1):159-66. PubMed ID: 8659521
    [Abstract] [Full Text] [Related]

  • 7. Isolation and strategies of novel tetranucleotide microsatellites with polymorphisms from different chromosomes of the rhesus monkey (Macaca mulatta).
    Xu Y, Hu Z, Li W, Zeng T, Zhang X, Li J, Zhang W, Yue B.
    Mol Biol Rep; 2019 Aug 01; 46(4):3955-3966. PubMed ID: 31119442
    [Abstract] [Full Text] [Related]

  • 8. Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I population.
    Peral B, Ward CJ, San Millán JL, Thomas S, Stallings RL, Moreno F, Harris PC.
    Am J Hum Genet; 1994 May 01; 54(5):899-908. PubMed ID: 7909986
    [Abstract] [Full Text] [Related]

  • 9. Microsatellites and Alu elements from the human MHC in Valencia (Spain): analysis of genetic relationships and linkage disequilibrium.
    García-Obregón S, Alfonso-Sánchez MA, Gómez-Pérez L, Pérez-Miranda AM, Arroyo D, de Pancorbo MM, Peña JA.
    Int J Immunogenet; 2011 Dec 01; 38(6):483-91. PubMed ID: 21933351
    [Abstract] [Full Text] [Related]

  • 10. A highly informative CA/GT repeat polymorphism in intron 38 of the human neurofibromatosis type 1 (NF1) gene.
    Lázaro C, Gaona A, Xu G, Weiss R, Estivill X.
    Hum Genet; 1993 Oct 01; 92(4):429-30. PubMed ID: 8225327
    [Abstract] [Full Text] [Related]

  • 11. A genetic study of neurofibromatosis type 1 (NF1) in south-western Ontario. II. A PCR based approach to molecular and prenatal diagnosis using linkage.
    Rodenhiser DI, Ainsworth PJ, Coulter-Mackie MB, Singh SM, Jung JH.
    J Med Genet; 1993 May 01; 30(5):363-8. PubMed ID: 8320697
    [Abstract] [Full Text] [Related]

  • 12. New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines.
    Banchs I, Bosch A, Guimerà J, Lázaro C, Puig A, Estivill X.
    Hum Mutat; 1994 May 01; 3(4):365-72. PubMed ID: 8081390
    [Abstract] [Full Text] [Related]

  • 13. Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping.
    Jorde LB, Watkins WS, Viskochil D, O'Connell P, Ward K.
    Am J Hum Genet; 1993 Nov 01; 53(5):1038-50. PubMed ID: 8105688
    [Abstract] [Full Text] [Related]

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  • 15. Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish population.
    Cobo A, Grinberg D, Balcells S, Vilageliu L, Gonzàlez-Duarte R, Baiget M.
    Hum Genet; 1992 May 01; 89(3):287-91. PubMed ID: 1351033
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  • 17. Four new DNA variants in the NF1 coding region.
    Wu R, Legius E.
    Genet Couns; 2000 May 01; 11(2):175-8. PubMed ID: 10893669
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  • 19. Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome.
    Hadj-Rabia S, Salomon R, Pelet A, Penet C, Rotschild A, de Laët MH, Chaouachi B, Hannachi R, Bakiri F, Brauner R, Chaussain JL, Munnich A, Lyonnet S.
    Eur J Hum Genet; 2000 Aug 01; 8(8):613-20. PubMed ID: 10951524
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