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Journal Abstract Search

187 related items for PubMed ID: 1683481

  • 1. Association between haplotypes and specific mutations in Swiss cystic fibrosis families.
    Liechti-Gallati S, Malik N, Alkan M, Maechler M, Morris M, Thonney F, Sennhauser F, Moser H.
    Pediatr Res; 1991 Oct; 30(4):304-8. PubMed ID: 1683481
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  • 3. Cystic fibrosis gene mutations and linked RFLPs in the Slovenian population.
    Ravnik-Glavac M, Gasparini P, Peterlin B, Strukelj M, Glavac D, Canki-Klain N, Pignatti PF, Komel R.
    Ann Genet; 1992 Oct; 35(2):85-8. PubMed ID: 1355957
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  • 4. [Molecular-genetic analysis of certain mutations of the "cystic fibrosis gene" in Moldavia. Characteristics of molecular markers and their linkage with various mutations].
    Gimbovskaia SD, Kalinin VN, Ivashchenko TE, Baranov VS.
    Genetika; 1994 Dec; 30(12):1616-20. PubMed ID: 7534245
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  • 9. Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patients.
    Wauters JG, Hendrickx J, Coucke P, Vits L, Stuer K, van Schil L, van der Auwera BJ, Van Elsen A, Dumon J, Willems PJ.
    Clin Genet; 1991 Feb; 39(2):89-92. PubMed ID: 1673094
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  • 11. Frequency of the delta F508 and exon 11 mutations in Norwegian cystic fibrosis patients.
    Eiklid K, Tranebjaerg L, Eiken HG, Pedersen JC, Michalsen H, Fluge G, Schwartz M, Nilsen BR, Bolle R, Skyberg D.
    Clin Genet; 1993 Jul; 44(1):12-4. PubMed ID: 7691448
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  • 12. 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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  • 16. The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and Arabs.
    Lerer I, Cohen S, Chemke M, Sanilevich A, Rivlin J, Golan A, Yahav J, Friedman A, Abeliovich D.
    Hum Genet; 1990 Sep 12; 85(4):416-7. PubMed ID: 1976595
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  • 17. Frequency of delta-F508 mutation and XV2C/KM19 haplotypes in Cuban cystic fibrosis families.
    Collazo T, Magarino C, Chavez R, Suardiaz B, Gispert S, Gomez M, Rojo M, Heredero L.
    Hum Hered; 1995 Sep 12; 45(1):55-7. PubMed ID: 7896301
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