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Journal Abstract Search

373 related items for PubMed ID: 1375186

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  • 2. Molecular and clinical findings in Austrian cystic fibrosis patients with mutations in exon 11 of the CFTR gene.
    Greil I, Wagner K, Eber E, Zach M, Rosenkranz W.
    Wien Klin Wochenschr; 1995; 107(15):464-9. PubMed ID: 7545856
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  • 7. Mutation analysis and haplotype correlation for 139 cystic fibrosis patients from the Nebraska Regional Cystic Fibrosis Center.
    Traystman MD, Schulte N, Colombo JL, Sammut PH, Reilly P, Patel C, Acquazzino D, Simanek B, Anderson R, Kimberling WJ.
    Hum Mutat; 1993; 2(1):7-15. PubMed ID: 7682884
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  • 9. [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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  • 15. 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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  • 16. Study of 12 mutations in Turkish cystic fibrosis patients.
    Yilmaz E, Erdem H, Ozgüç M, Coşkun T, Ozçelik U, Göçmen A, Ozalp I.
    Hum Hered; 1995 Jul; 45(3):175-7. PubMed ID: 7542223
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  • 18. Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutation.
    Kanavakis E, Tzetis M, Antoniadi T, Traeger-Synodinos J, Doudounakis S, Adam G, Matsaniotis N, Kattamis C.
    Hum Genet; 1995 Sep; 96(3):364-6. PubMed ID: 7544320
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  • 20. Distribution of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations in a Cohort of Patients Residing in Palestine.
    Siryani I, Jama M, Rumman N, Marzouqa H, Kannan M, Lyon E, Hindiyeh M.
    PLoS One; 2015 Sep; 10(7):e0133890. PubMed ID: 26208274
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