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Journal Abstract Search

110 related items for PubMed ID: 7899288

  • 1. Compound heterozygosity for delta F508 and F508C: a cautionary note on the molecular diagnosis of cystic fibrosis.
    Dufourcq R, Vuillaumier S, Pascaud O, Guidal C, Oury JF, Elion J, Denamur E.
    Prenat Diagn; 1994 Dec; 14(12):1176-7. PubMed ID: 7899288
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  • 2. Molecular screening of cystic fibrosis patients.
    Fellowes AP, Murphy JM, Wesley AW, Dawson KP, George PM.
    N Z Med J; 1991 Oct 09; 104(921):415-6. PubMed ID: 1923090
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  • 4. Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (delta F508).
    Cui KH, Haan EA, Wang LJ, Matthews CD.
    BMJ; 1995 Aug 26; 311(7004):536-40. PubMed ID: 7545043
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  • 6. [Analysis of five mutations of cystic fibrosis occurring in the Hungarian population].
    Németh K, Holics K, Ujhelyi R, Váradi A, Fekete G.
    Orv Hetil; 1996 Apr 28; 137(17):899-903. PubMed ID: 8649752
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  • 15. Benign missense variations in the cystic fibrosis gene.
    Kobayashi K, Knowles MR, Boucher RC, O'Brien WE, Beaudet AL.
    Am J Hum Genet; 1990 Oct 28; 47(4):611-5. PubMed ID: 1977306
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  • 17. [A 13-year-old boy with a mild form of cystic fibrosis and heterozygote gene mutation for Delta F508].
    Hiort O, Artlich A, Wiebicke W.
    Pneumologie; 1991 Nov 28; 45(11):910-2. PubMed ID: 1763003
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