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Journal Abstract Search

187 related items for PubMed ID: 12624947

  • 1. [The mutation spectrum of the CFTR gene in mucoviscidosis patients from Bashkortostan].
    Korytina GF, Viktorova TV, Ivashchenko TE, Baranov VS, Khusnutdinova EK.
    Mol Biol (Mosk); 2003; 37(1):61-7. PubMed ID: 12624947
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  • 2. [Analysis of the spectra of mutations and polymorphic loci of cystic fibrosis transmembrane conductance regulator in the population of Bashkortostan].
    Korytina GF, Viktorova TV, Baĭkova GV, Khusnutdinova EK.
    Genetika; 2002 Sep; 38(9):1270-5. PubMed ID: 12391889
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  • 4. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
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  • 5. Mutation analysis of CFTR gene in 70 Iranian cystic fibrosis patients.
    Alibakhshi R, Zamani M.
    Iran J Allergy Asthma Immunol; 2006 Mar; 5(1):3-8. PubMed ID: 17242497
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  • 6. [The frequency and spectrum of mutations and the IVS8-T polymorphism of the CFTR gene in Russian infertile men].
    Chernykh VB, Stepanova AA, Beskorovaĭnaia TS, Sorokina TM, Shileĭko LV, Kurilo LF, Poliakov AV.
    Genetika; 2010 Jun; 46(6):844-52. PubMed ID: 20734777
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  • 7. CFTR gene analysis in cystic fibrosis patients: detection of 91% of molecular defects and identification of the novel mutation D979V.
    Plouvier E, Cougoureux E, Sardet A, Tournier G, Aymard P, Feldmann D.
    Ann Genet; 1997 Jun; 40(3):185-8. PubMed ID: 9401110
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  • 9. Two new mutations (1811 + 1G-->C and Y569C) identified in the CFTR gene in patients of Macedonian and Croatian origin.
    Petreska L, Plaseska D, Koceva S, Stavljenić-Rukavina A, Efremov GD.
    Acta Med Croatica; 1996 Jun; 50(3):125-7. PubMed ID: 8890528
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  • 10. Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel alleles.
    Verlingue C, Kapranov NI, Mercier B, Ginter EK, Petrova NV, Audrezet MP, Férec C.
    Hum Mutat; 1995 Jun; 5(3):205-9. PubMed ID: 7541273
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  • 11. High heterogeneity of CFTR mutations and unexpected low incidence of cystic fibrosis in the Mediterranean France.
    des Georges M, Guittard C, Altiéri JP, Templin C, Sarles J, Sarda P, Claustres M.
    J Cyst Fibros; 2004 Dec; 3(4):265-72. PubMed ID: 15698946
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  • 15. [Reliability of the Search for 19 Common Mutations in the CFTR Gene in Russian Cystic Fibrosis Patients and the Calculated Frequency of the Disease in Russian Federation].
    Stepanova AA, Krasovsky SA, Polyakov AV.
    Genetika; 2016 Feb; 52(2):231-41. PubMed ID: 27215038
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  • 16. Diagnostic usefulness of the polymorphism of the GT dinucleotide and the polythymidine tract in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Cazeneuve C, Beldjord C, Kaplan JC, Bienvenu T.
    Ann Genet; 1995 Feb; 38(4):202-5. PubMed ID: 8629807
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  • 18. Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosis.
    Ko JM, Kim GH, Kim KM, Hong SJ, Yoo HW.
    J Korean Med Sci; 2008 Oct; 23(5):912-5. PubMed ID: 18955805
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  • 20. The study of cystic fibrosis transmembrane conductance regulator gene mutations in a group of patients from Romania.
    Frenţescu L, Brownsell E, Hinks J, Malone G, Shaw H, Budişan L, Bulman M, Schwarz M, Pop L, Filip M, Tomescu E, Moşescu S, Popa I, Benga G.
    J Cyst Fibros; 2008 Sep; 7(5):423-8. PubMed ID: 18467194
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