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.
131 related articles for article (PubMed ID: 10970190)
1. Many deltaF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation. Boyne J; Evans S; Pollitt RJ; Taylor CJ; Dalton A J Med Genet; 2000 Jul; 37(7):543-7. PubMed ID: 10970190 [No Abstract] [Full Text] [Related]
2. Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in neonatal hypertrypsinaemia with normal sweat test. Castellani C; Benetazzo MG; Tamanini A; Begnini A; Mastella G; Pignatti P J Med Genet; 2001 Mar; 38(3):202-5. PubMed ID: 11303517 [No Abstract] [Full Text] [Related]
3. Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis. Scotet V; De Braekeleer M; Audrézet MP; Lodé L; Verlingue C; Quéré I; Mercier B; Duguépéroux I; Codet JP; Moineau MP; Parent P; Férec C Clin Genet; 2001 Jan; 59(1):42-7. PubMed ID: 11168024 [TBL] [Abstract][Full Text] [Related]
5. Prenatal and newborn screening for CFTR mutations: the difficulties of prediction. Schwarz MJ Clin Biochem; 2011 May; 44(7):485-486. PubMed ID: 22036338 [No Abstract] [Full Text] [Related]
6. Distribution of CFTR gene mutations in cystic fibrosis patients from Estonia. Teder M; Klaassen T; Oitmaa E; Kaasik K; Metspalu A J Med Genet; 2000 Aug; 37(8):E16. PubMed ID: 10922396 [No Abstract] [Full Text] [Related]
7. Identification of the L927P and delta L1260 mutations in the CFTR gene. Hermans CJ; Veeze HJ; Drexhage VR; Halley DJ; van den Ouweland AM Hum Mol Genet; 1994 Jul; 3(7):1199-200. PubMed ID: 7526927 [No Abstract] [Full Text] [Related]
9. A continuing role for sweat testing in an era of newborn screening for cystic fibrosis. Kirk JM Clin Biochem; 2011 May; 44(7):487-488. PubMed ID: 22036339 [No Abstract] [Full Text] [Related]
10. CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test. Castellani C; Bonizzato A; Mastella G J Med Genet; 1997 Apr; 34(4):297-301. PubMed ID: 9138152 [TBL] [Abstract][Full Text] [Related]
11. Population screening of F508del (DeltaF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina. Roqué M; Godoy CP; Castellanos M; Pusiol E; Mayorga LS Hum Mutat; 2001 Aug; 18(2):167. PubMed ID: 11462248 [TBL] [Abstract][Full Text] [Related]
12. [Systematic neonatal screening]. Guillot M; Travert G; Roussey M; Figarella C; Vidailhet M Arch Pediatr; 2001 Dec; 8 Suppl 5():833s-837s. PubMed ID: 11811052 [No Abstract] [Full Text] [Related]
14. Identification of the commonest cystic fibrosis transmembrane regulator gene DeltaF508 mutation: evaluation of PCR--single-strand conformational polymorphism and polyacrylamide gel electrophoresis. Kakavas KV; Noulas AV; Kanakis I; Bonanou S; Karamanos NK Biomed Chromatogr; 2006 Oct; 20(10):1120-5. PubMed ID: 16708396 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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 [TBL] [Abstract][Full Text] [Related]
17. Is the spectrum of mutations in Indian patients with cystic fibrosis different? Kabra M; Kabra SK; Ghosh M; Khanna A; Arora S; Menon PS; Verma IC; Wallace A Am J Med Genet; 2000 Jul; 93(2):161-3. PubMed ID: 10869121 [No Abstract] [Full Text] [Related]