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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

92 related items for PubMed ID: 8364537

  • 1. Haplotype analysis to determine the position of a mutation among closely linked DNA markers.
    Ramsay M, Williamson R, Estivill X, Wainwright BJ, Ho MF, Halford S, Kere J, Savilahti E, de la Chapelle A, Schwartz M.
    Hum Mol Genet; 1993 Jul; 2(7):1007-14. PubMed ID: 8364537
    [Abstract] [Full Text] [Related]

  • 2. Patterns of polymorphism and linkage disequilibrium for cystic fibrosis.
    Estivill X, Scambler PJ, Wainwright BJ, Hawley K, Frederick P, Schwartz M, Baiget M, Kere J, Williamson R, Farrall M.
    Genomics; 1987 Nov; 1(3):257-63. PubMed ID: 2895728
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population.
    Vidaud M, Kitzis A, Ferec C, Bozon D, Dumur V, Giraud G, David F, Pascal O, Auvinet M, Morel Y.
    Hum Genet; 1989 Jan; 81(2):183-4. PubMed ID: 2563252
    [Abstract] [Full Text] [Related]

  • 5. Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations of the cystic fibrosis gene.
    Cutting GR, Antonarakis SE, Buetow KH, Kasch LM, Rosenstein BJ, Kazazian HH.
    Am J Hum Genet; 1989 Mar; 44(3):307-18. PubMed ID: 2563631
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP.
    Estivill X, McLean C, Nunes V, Casals T, Gallano P, Scambler P, Williamson R.
    Am J Hum Genet; 1989 May; 44(5):704-10. PubMed ID: 2565082
    [Abstract] [Full Text] [Related]

  • 8. Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study.
    Estivill X, Farrall M, Williamson R, Ferrari M, Seia M, Giunta AM, Novelli G, Potenza L, Dallapicolla B, Borgo G.
    Am J Hum Genet; 1988 Jul; 43(1):23-8. PubMed ID: 2897786
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. [Portion of certain cystic fibrosis gene mutations and linkage dysequilibrium between the CFTR-gene locus and two DNA marker loci in Russian populations].
    Petrova NV, Ginter EK, Kapranov NI, El'chinova GI.
    Genetika; 1994 Jul; 30(7):974-7. PubMed ID: 7525404
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populations.
    Estivill X, Gasparini P, Novelli G, Casals T, Nunes V, Gallano P, Savoia A, Ruzzo A, Dallapiccola B, Pignatti PF.
    Hum Genet; 1989 Sep; 83(2):175-8. PubMed ID: 2777258
    [Abstract] [Full Text] [Related]

  • 16. [Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region].
    Sazonova MA, Amosenko FA, Kapranov NI, Kalinin VN.
    Genetika; 1997 Sep; 33(9):1303-7. PubMed ID: 9445824
    [Abstract] [Full Text] [Related]

  • 17. Haplotypes in cystic fibrosis patients with or without pancreatic insufficiency from four European populations.
    Devoto M, De Benedetti L, Seia M, Piceni Sereni L, Ferrari M, Bonduelle ML, Malfroot A, Lissens W, Balassopoulou A, Adam G.
    Genomics; 1989 Nov; 5(4):894-8. PubMed ID: 2574150
    [Abstract] [Full Text] [Related]

  • 18. Classifying disease chromosomes arising from multiple founders, with application to fine-scale haplotype mapping.
    Yu K, Martin RB, Whittemore AS.
    Genet Epidemiol; 2004 Nov; 27(3):173-81. PubMed ID: 15389930
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.