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470 related items for PubMed ID: 17560176

  • 1. ENaCbeta and gamma genes as modifier genes in cystic fibrosis.
    Viel M, Leroy C, Hubert D, Fajac I, Bienvenu T.
    J Cyst Fibros; 2008 Jan; 7(1):23-9. PubMed ID: 17560176
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  • 2. Genotype-phenotype correlation for pulmonary function in cystic fibrosis.
    de Gracia J, Mata F, Alvarez A, Casals T, Gatner S, Vendrell M, de la Rosa D, Guarner L, Hermosilla E.
    Thorax; 2005 Jul; 60(7):558-63. PubMed ID: 15994263
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  • 3. Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes.
    Salvatore F, Scudiero O, Castaldo G.
    Am J Med Genet; 2002 Jul 22; 111(1):88-95. PubMed ID: 12124743
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  • 10. Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations.
    Geborek A, Hjelte L.
    J Cyst Fibros; 2011 May 22; 10(3):187-92. PubMed ID: 21354377
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  • 12. Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease.
    Azad AK, Rauh R, Vermeulen F, Jaspers M, Korbmacher J, Boissier B, Bassinet L, Fichou Y, des Georges M, Stanke F, De Boeck K, Dupont L, Balascáková M, Hjelte L, Lebecque P, Radojkovic D, Castellani C, Schwartz M, Stuhrmann M, Schwarz M, Skalicka V, de Monestrol I, Girodon E, Férec C, Claustres M, Tümmler B, Cassiman JJ, Korbmacher C, Cuppens H.
    Hum Mutat; 2009 Jul 22; 30(7):1093-103. PubMed ID: 19462466
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  • 13. Genotype-phenotype correlation in cystic fibrosis patients.
    Ferrari M, Cremonesi L.
    Ann Biol Clin (Paris); 1996 Jul 22; 54(6):235-41. PubMed ID: 8949420
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  • 16. Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.
    Stanke F, Ballmann M, Bronsveld I, Dörk T, Gallati S, Laabs U, Derichs N, Ritzka M, Posselt HG, Harms HK, Griese M, Blau H, Mastella G, Bijman J, Veeze H, Tümmler B.
    J Med Genet; 2008 Jan 22; 45(1):47-54. PubMed ID: 18178635
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  • 17. Familial concordance of phenotype and microbial variation among siblings with CF.
    Picard E, Aviram M, Yahav Y, Rivlin J, Blau H, Bentur L, Avital A, Villa Y, Schwartz S, Kerem B, Kerem E.
    Pediatr Pulmonol; 2004 Oct 22; 38(4):292-7. PubMed ID: 15334505
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  • 18. Genotype-phenotype relationship for five CFTR mutations frequently identified in western France.
    Duguépéroux I, De Braekeleer M, Participating Centres to the French National Cystic Fibrosis Registry.
    J Cyst Fibros; 2004 Dec 22; 3(4):259-63. PubMed ID: 15698945
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  • 19. Association of improved pulmonary phenotype in Irish cystic fibrosis patients with a 3' enhancer polymorphism in alpha-1-antitrypsin.
    Courtney JM, Plant BJ, Morgan K, Rendall J, Gallagher C, Ennis M, Kalsheker N, Elborn S, O'Connor CM.
    Pediatr Pulmonol; 2006 Jun 22; 41(6):584-91. PubMed ID: 16617455
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