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13. Segregation analysis in cystic fibrosis at-risk family demonstrates that the M348K CFTR mutation is a rare innocuous polymorphism. D'Apice MR; Gambardella S; Russo S; Lucidi V; Nardone AM; Pietropolli A; Novelli G Prenat Diagn; 2004 Dec; 24(12):981-3. PubMed ID: 15614862 [TBL] [Abstract][Full Text] [Related]
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16. [Correlation between phenotype and genotype in a group of patients with cystic fibrosis]. Navarro H; Kolbach M; Repetto G; Guiraldes E; Harris P; Foradori A; Poggi H; Sánchez I Rev Med Chil; 2002 May; 130(5):475-81. PubMed ID: 12143267 [TBL] [Abstract][Full Text] [Related]
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19. Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian population. Castaldo G; Polizzi A; Tomaiuolo R; Cazeneuve C; Girodon E; Santostasi T; Salvatore D; Raia V; Rigillo N; Goossens M; Salvatore F Ann Hum Genet; 2005 Jan; 69(Pt 1):15-24. PubMed ID: 15638824 [TBL] [Abstract][Full Text] [Related]
20. Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosis. Rabbi-Bortolini E; Bernardino AL; Lopes AL; Ferri AS; Passos-Bueno MR; Zatz M Am J Med Genet; 1998 Apr; 76(4):288-90. PubMed ID: 9545091 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]