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Journal Abstract Search

95 related items for PubMed ID: 2882884

  • 21. [Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].
    Iwańczak F, Smigiel R, Stawarski A, Pawłowicz J, Stembalska A, Mowszet K, Sasiadek M.
    Pol Merkur Lekarski; 2005 Feb; 18(104):205-9. PubMed ID: 17877132
    [Abstract] [Full Text] [Related]

  • 22. [Genetic diagnosis for inherited lung disorders].
    Kanda A, Ueki S, Chihara J.
    Rinsho Byori; 2002 Nov; Suppl 123():178-83. PubMed ID: 12652807
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  • 23. [Genetic variation and genetic diseases].
    Børresen AL, Berg K.
    Tidsskr Nor Laegeforen; 1989 Oct 20; 109(29):3003-9. PubMed ID: 2588229
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  • 24. [Prenatal diagnosis of cystic fibrosis with recombinant DNA methods].
    Schmidtke J, Krawczak M.
    Monatsschr Kinderheilkd; 1987 Dec 20; 135(12):805-10. PubMed ID: 3481436
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  • 25. [Molecular biology and mucoviscidosis. Brest experience in 1987].
    Parent P, Ferec C, Jehanne M, Chabaud JJ, Boog G, Saleun JP, Alix D.
    Arch Fr Pediatr; 1988 May 20; 45(5):319-22. PubMed ID: 3415412
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  • 26. Human Genome Project and cystic fibrosis--a symbiotic relationship.
    Tolstoi LG, Smith CL.
    J Am Diet Assoc; 1999 Nov 20; 99(11):1421-7. PubMed ID: 10570680
    [Abstract] [Full Text] [Related]

  • 27. Association of common haplotypes of surfactant protein A1 and A2 (SFTPA1 and SFTPA2) genes with severity of lung disease in cystic fibrosis.
    Choi EH, Ehrmantraut M, Foster CB, Moss J, Chanock SJ.
    Pediatr Pulmonol; 2006 Mar 20; 41(3):255-62. PubMed ID: 16429424
    [Abstract] [Full Text] [Related]

  • 28. Association of improved pulmonary phenotype in Irish cystic fibrosis patients with a 3' enhancer polymorphism in alpha-1-antitrypsin.
    Courtney JM, Plant BJ, Morgan K, Rendall J, Gallagher C, Ennis M, Kalsheker N, Elborn S, O'Connor CM.
    Pediatr Pulmonol; 2006 Jun 20; 41(6):584-91. PubMed ID: 16617455
    [Abstract] [Full Text] [Related]

  • 29. Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded.
    De bruyn A, Raeymaekers P, Mendelbaum K, Sandkuijl LA, Raes G, Delvenne V, Hirsch D, Staner L, Mendlewicz J, Van Broeckhoven C.
    Am J Med Genet; 1994 Dec 15; 54(4):411-9. PubMed ID: 7726217
    [Abstract] [Full Text] [Related]

  • 30. Positional cloning approach to the dominant polycystic kidney disease gene, PKD1.
    Germino GG, Somlo S, Weinstat-Saslow D, Reeders ST.
    Kidney Int Suppl; 1993 Jan 15; 39():S20-5. PubMed ID: 8468920
    [Abstract] [Full Text] [Related]

  • 31. Search for the familial Alzheimer's disease gene.
    St George-Hyslop P, Polinsky R, Haines J, Nee L, Tanzi R, Conneally P, Growdon J, Myers R, Pollen D, Drachman D.
    J Neural Transm Suppl; 1987 Jan 15; 24():13-21. PubMed ID: 2890708
    [Abstract] [Full Text] [Related]

  • 32. Approaches to localizing disease genes as applied to cystic fibrosis.
    Dean M, Drumm ML, Stewart C, Gerrard B, Perry A, Hidaka N, Cole JL, Collins FS, Iannuzzi MC.
    Nucleic Acids Res; 1990 Jan 25; 18(2):345-50. PubMed ID: 1970161
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  • 37. Cystic fibrosis carrier detection using a linked gene probe.
    Farrall M, Scambler P, Klinger KW, Davies K, Worrall C, Williamson R, Wainwright B.
    J Med Genet; 1986 Aug 25; 23(4):295-9. PubMed ID: 3018247
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