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Journal Abstract Search

147 related items for PubMed ID: 9628826

  • 21. [Characteristics and specificities of cystic fibrosis in adults: evolutive disease of childhood or recently diagnosed disease?].
    Hubert D, Rivoal V, Desmazes-Dufeu N, Lacronique J, Maurer C, Richaud-Thiriez B, Dusser D.
    Rev Mal Respir; 2000 Aug; 17(3 Pt 2):749-57. PubMed ID: 11076385
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  • 23. Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis.
    Moutou C, Gardes N, Viville S.
    Eur J Hum Genet; 2002 Apr; 10(4):231-8. PubMed ID: 12032730
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  • 24. Cystic Fibrosis in Ukraine: age, origin and tracing of the delta F508 mutation.
    Livshits LA, Kravchenko SA.
    Gene Geogr; 1996 Dec; 10(3):219-27. PubMed ID: 9263776
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  • 32. Sequence of deltaF508 CFTR allele identified at present is lacking in medieval specimens from Central Poland. Preliminary results.
    Witas HW, Jatczak I, Jedrychowska-Dańska K, Zadzińska E, Wrzesińska A, Wrzesiński J, Nadolski J.
    Anthropol Anz; 2006 Mar; 64(1):41-9. PubMed ID: 16623087
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  • 33. Characterisation of mutations and genotype-phenotype correlation in cystic fibrosis: experience from India.
    Shastri SS, Kabra M, Kabra SK, Pandey RM, Menon PS.
    J Cyst Fibros; 2008 Mar; 7(2):110-5. PubMed ID: 17716958
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  • 34. DeltaF508 heterozygosity in cystic fibrosis and susceptibility to asthma.
    Dahl M, Tybjaerg-Hansen A, Lange P, Nordestgaard BG.
    Lancet; 1998 Jun 27; 351(9120):1911-3. PubMed ID: 9654257
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  • 36. The cystic fibrosis delta F508 gene mutation and cancer.
    Padua RA, Warren N, Grimshaw D, Smith M, Lewis C, Whittaker J, Laidler P, Wright P, Douglas-Jones A, Fenaux P, Sharma A, Horgan K, West R.
    Hum Mutat; 1997 Jun 27; 10(1):45-8. PubMed ID: 9222759
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  • 37. Asthma and COPD in cystic fibrosis intron-8 5T carriers. A population-based study.
    Dahl M, Tybjaerg-Hansen A, Lange P, Nordestgaard BG.
    Respir Res; 2005 Oct 09; 6(1):113. PubMed ID: 16212675
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  • 40. A pilot survey of cystic fibrosis clinical manifestations in CFTR mutation heterozygotes.
    Castellani C, Quinzii C, Altieri S, Mastella G, Assael BM.
    Genet Test; 2001 Oct 09; 5(3):249-54. PubMed ID: 11788092
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