These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. Screening for mutations in the cystic fibrosis transmembrane regulator gene in an infertility clinic. Slostad J; Stein QP; Flanagan JD; Hansen KA Fertil Steril; 2007 Dec; 88(6):1687-8. PubMed ID: 17482604 [TBL] [Abstract][Full Text] [Related]
5. 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 [TBL] [Abstract][Full Text] [Related]
7. [Aquagenic wrinkling of the palms in a patient with cystic fibrosis heterozygous for the DeltaF 508 mutation]. Garçon N; Roguedas AM; Misery L; Audrezet MP; Ferec C Ann Dermatol Venereol; 2008 Mar; 135(3):232-4. PubMed ID: 18374861 [No Abstract] [Full Text] [Related]
9. Cystic fibrosis in a boy with meconium ileus and mild clinical phenotype associated with 2183AA-G/D1152H genotype. Yalçin E; Ozçelik U; Yilmaz E; Doğru D; Kiper N; Ferec C Turk J Pediatr; 2008; 50(4):383-5. PubMed ID: 19014055 [TBL] [Abstract][Full Text] [Related]
10. Phenotype expression in a case of adult cystic fibrosis caused by an extremely rare compound heterozygous genotype (2183AA>G/2789+5G>A). Capurso G; Sbrozzi-Vanni A; Piane M; Begini P; Panzuto F; Libi F; Margagnoni G; Capotondi C; Marignani M; Chessa L; Delle Fave G Pancreas; 2009 Jul; 38(5):599-601. PubMed ID: 19550280 [No Abstract] [Full Text] [Related]
12. Newborn screening for cystic fibrosis in New York State. Caggana M; Helton L Pediatrics; 2007 Jul; 120(1):241; author reply 241-3. PubMed ID: 17606589 [No Abstract] [Full Text] [Related]
13. Cystic fibrosis heterozygotes do not have increased platelet activation. Tarnow I; Michelson AD; Frelinger AL; Linden MD; Li Y; Fox ML; Barnard MR; O'Sullivan BP Thromb Res; 2007; 121(2):159-62. PubMed ID: 17532368 [TBL] [Abstract][Full Text] [Related]
14. Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene. Brugnon F; Bilan F; Heraud MC; Grizard G; Janny L; Creveaux I Fertil Steril; 2008 Nov; 90(5):2004.e23-6. PubMed ID: 18703181 [TBL] [Abstract][Full Text] [Related]
15. Potential role of the "NADPH oxidases" (NOX/DUOX) family in cystic fibrosis. Pongnimitprasert N; El-Benna J; Foglietti MJ; Gougerot-Pocidalo MA; Bernard M; Braut-Boucher F Ann Biol Clin (Paris); 2008; 66(6):621-9. PubMed ID: 19091660 [TBL] [Abstract][Full Text] [Related]
16. Cystic fibrosis: refining the approach to newborn screening. Wilcken B J Pediatr; 2009 Nov; 155(5):605-6. PubMed ID: 19840611 [No Abstract] [Full Text] [Related]
17. [3120+1kbdel8.6kb]+[p.N1303K] genotype in an Emirati cystic fibrosis patient: indication of a founder mutation in Palestinian Arabs. Saleheen D; Frossard PM; Girodon E J Ayub Med Coll Abbottabad; 2006; 18(3):69-71. PubMed ID: 17348320 [TBL] [Abstract][Full Text] [Related]
18. Increased arylsulfatase B activity in cystic fibrosis cells following correction of CFTR. Bhattacharyya S; Look D; Tobacman JK Clin Chim Acta; 2007 May; 380(1-2):122-7. PubMed ID: 17324393 [TBL] [Abstract][Full Text] [Related]
19. Negative genetic neonatal screening for cystic fibrosis caused by compound heterozygosity for two large CFTR rearrangements. Girardet A; Guittard C; Altieri JP; Templin C; Stremler N; Beroud C; des Georges M; Claustres M Clin Genet; 2007 Oct; 72(4):374-7. PubMed ID: 17850636 [No Abstract] [Full Text] [Related]
20. Phenotypic variability in a family with pancreatitis and cystic fibrosis sharing common mild CFTR mutation: report on CFTR mutations and their phenotypic variability. Alghisi F; Bella S; Lucidi V; Angioni A; Tomaiuolo AC; D'Apice MR; Gambardella S; Novelli G Pancreas; 2009 Jan; 38(1):109-10. PubMed ID: 19106752 [No Abstract] [Full Text] [Related] [Next] [New Search]