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Journal Abstract Search

165 related items for PubMed ID: 20051989

  • 21. Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.
    Dörk T, Neumann T, Wulbrand U, Wulf B, Kälin N, Maass G, Krawczak M, Guillermit H, Ferec C, Horn G.
    Hum Genet; 1992 Feb; 88(4):417-25. PubMed ID: 1371263
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  • 22. Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.
    Morral N, Nunes V, Casals T, Chillón M, Giménez J, Bertranpetit J, Estivill X.
    Hum Mol Genet; 1993 Jul; 2(7):1015-22. PubMed ID: 7689896
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  • 23. Association of IVS6A GATT polymorphism of CFTR gene with cystic fibrosis: first study in CF and normal Tunisian population.
    Chaima S, Sondess HF, Khedija B, Ahmed M, Taieb M.
    Ann Biol Clin (Paris); 2020 Jun 01; 78(3):314-318. PubMed ID: 32540817
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  • 24. Cystic fibrosis: S158N (605G --> A) is a rare genetic variant found in coupling with deltaF508.
    Hicks K, Beadling W, Shrimpton AE.
    Genet Test; 2003 Jun 01; 7(1):73-6. PubMed ID: 12820707
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  • 25. Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia.
    Brucato N, DeLisi LE, Fisher SE, Francks C.
    Am J Med Genet B Neuropsychiatr Genet; 2014 Oct 01; 165B(7):555-63. PubMed ID: 25111784
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  • 26. Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis.
    Blackman SM, Deering-Brose R, McWilliams R, Naughton K, Coleman B, Lai T, Algire M, Beck S, Hoover-Fong J, Hamosh A, Fallin MD, West K, Arking DE, Chakravarti A, Cutler DJ, Cutting GR.
    Gastroenterology; 2006 Oct 01; 131(4):1030-9. PubMed ID: 17030173
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  • 27. Linkage disequilibrium between cystic fibrosis mutations and polymorphic 4-bp repeat within CFTR gene.
    Gaitskhoki VS, Voronina OV, Potapova OYu, Kirjukhina LV, Gembitskaya TE, Kapranov NI, Petrova NV, Khafizova ZA, Schwartz EI.
    Biochem Med Metab Biol; 1993 Oct 01; 50(2):186-9. PubMed ID: 7505092
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  • 28. Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulator.
    Mekus F, Ballmann M, Bronsveld I, Dörk T, Bijman J, Tümmler B, Veeze HJ.
    Hum Genet; 1998 May 01; 102(5):582-6. PubMed ID: 9654209
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  • 29. A frame-shift mutation in the cystic fibrosis gene.
    White MB, Amos J, Hsu JM, Gerrard B, Finn P, Dean M.
    Nature; 1990 Apr 12; 344(6267):665-7. PubMed ID: 1691449
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  • 30. Phenotypic discordance in three siblings affected by atypical cystic fibrosis with the F508del/D614G genotype.
    Castaldo G, Tomaiuolo R, Vanacore B, Ferrara P, DEL Vecchio S, Carnovale V, Abete P, Rengo F, Salvatore F.
    J Cyst Fibros; 2006 Aug 12; 5(3):193-5. PubMed ID: 16478680
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  • 32. Genetic modifiers of nutritional status in cystic fibrosis.
    Bradley GM, Blackman SM, Watson CP, Doshi VK, Cutting GR.
    Am J Clin Nutr; 2012 Dec 12; 96(6):1299-308. PubMed ID: 23134884
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  • 40. Tandem repeats in the CpG islands of imprinted genes.
    Hutter B, Helms V, Paulsen M.
    Genomics; 2006 Sep 12; 88(3):323-32. PubMed ID: 16690248
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