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5. Variant cystic fibrosis phenotypes in the absence of CFTR mutations. Groman JD; Meyer ME; Wilmott RW; Zeitlin PL; Cutting GR N Engl J Med; 2002 Aug; 347(6):401-7. PubMed ID: 12167682 [TBL] [Abstract][Full Text] [Related]
6. Bronchiectasis in adult patients: an expression of heterozygosity for CFTR gene mutations? Casals T; De-Gracia J; Gallego M; Dorca J; Rodríguez-Sanchón B; Ramos MD; Giménez J; Cisteró-Bahima A; Olveira C; Estivill X Clin Genet; 2004 Jun; 65(6):490-5. PubMed ID: 15151509 [TBL] [Abstract][Full Text] [Related]
7. [Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis]. Iwańczak F; Smigiel R; Stawarski A; Pawłowicz J; Stembalska A; Mowszet K; Sasiadek M Pol Merkur Lekarski; 2005 Feb; 18(104):205-9. PubMed ID: 17877132 [TBL] [Abstract][Full Text] [Related]
8. Lack of association of common cystic fibrosis transmembrane conductance regulator gene mutations with primary sclerosing cholangitis. Gallegos-Orozco JF; E Yurk C; Wang N; Rakela J; Charlton MR; Cutting GR; Balan V Am J Gastroenterol; 2005 Apr; 100(4):874-8. PubMed ID: 15784035 [TBL] [Abstract][Full Text] [Related]
9. [Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis]. Radivojević D; Guć-Sćekić M; Djurisić M; Lalić T; Minić P; Kanavakis E Srp Arh Celok Lek; 2001; 129 Suppl 1():6-9. PubMed ID: 15637983 [TBL] [Abstract][Full Text] [Related]
10. Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. Castellani C; Gomez Lira M; Frulloni L; Delmarco A; Marzari M; Bonizzato A; Cavallini G; Pignatti P; Mastella G Hum Mutat; 2001 Aug; 18(2):166. PubMed ID: 11462247 [TBL] [Abstract][Full Text] [Related]
11. Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France. Claustres M; Guittard C; Bozon D; Chevalier F; Verlingue C; Ferec C; Girodon E; Cazeneuve C; Bienvenu T; Lalau G; Dumur V; Feldmann D; Bieth E; Blayau M; Clavel C; Creveaux I; Malinge MC; Monnier N; Malzac P; Mittre H; Chomel JC; Bonnefont JP; Iron A; Chery M; Georges MD Hum Mutat; 2000; 16(2):143-56. PubMed ID: 10923036 [TBL] [Abstract][Full Text] [Related]
12. 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 [TBL] [Abstract][Full Text] [Related]
13. Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis. Cohn JA; Friedman KJ; Noone PG; Knowles MR; Silverman LM; Jowell PS N Engl J Med; 1998 Sep; 339(10):653-8. PubMed ID: 9725922 [TBL] [Abstract][Full Text] [Related]
14. Missense mutations in the cystic fibrosis gene in adult patients with asthma. Lázaro C; de Cid R; Sunyer J; Soriano J; Giménez J; Alvarez M; Casals T; Antó JM; Estivill X Hum Mutat; 1999; 14(6):510-9. PubMed ID: 10571949 [TBL] [Abstract][Full Text] [Related]
15. Improved detection of CFTR mutations in Southern California Hispanic CF patients. Wong LJ; Wang J; Zhang YH; Hsu E; Heim RA; Bowman CM; Woo MS Hum Mutat; 2001 Oct; 18(4):296-307. PubMed ID: 11668613 [TBL] [Abstract][Full Text] [Related]
16. Improved detection of cystic fibrosis mutations in infertility patients with DNA sequence analysis. Danziger KL; Black LD; Keiles SB; Kammesheidt A; Turek PJ Hum Reprod; 2004 Mar; 19(3):540-6. PubMed ID: 14998948 [TBL] [Abstract][Full Text] [Related]
17. CFTR genotypes in patients with normal or borderline sweat chloride levels. Feldmann D; Couderc R; Audrezet MP; Ferec C; Bienvenu T; Desgeorges M; Claustres M; Mittre H; Blayau M; Bozon D; Malinge MC; Monnier N; Bonnefont JP; Iron A; Bieth E; Dumur V; Clavel C; Cazeneuve C; Girodon E Hum Mutat; 2003 Oct; 22(4):340. PubMed ID: 12955726 [TBL] [Abstract][Full Text] [Related]
18. [Molecular basis of phenotype heterogeneity in cystic fibrosis]. Bienvenu T Ann Biol Clin (Paris); 1997; 55(2):113-21. PubMed ID: 9180964 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Prospective analysis of cystic fibrosis transmembrane regulator mutations in adults with bronchiectasis or pulmonary nontuberculous mycobacterial infection. Ziedalski TM; Kao PN; Henig NR; Jacobs SS; Ruoss SJ Chest; 2006 Oct; 130(4):995-1002. PubMed ID: 17035430 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]