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.
114 related articles for article (PubMed ID: 7599637)
1. A single-tube multiplex system for the simultaneous detection of 10 common cystic fibrosis mutations. Axton RA; Brock DJ Hum Mutat; 1995; 5(3):260-2. PubMed ID: 7599637 [TBL] [Abstract][Full Text] [Related]
2. Mutation analysis of 184 cystic fibrosis families in Wales. Cheadle J; Myring J; al-Jader L; Meredith L J Med Genet; 1992 Sep; 29(9):642-6. PubMed ID: 1357180 [TBL] [Abstract][Full Text] [Related]
3. [Genetic testing for cystic fibrosis: evaluation of the Elucigene CF20 kit in blood and buccal cells]. Feldmann D; Guittard C; Georges MD; Houdayer C; Magnier C; Claustres M; Couderc R Ann Biol Clin (Paris); 2001; 59(3):277-83. PubMed ID: 11397675 [TBL] [Abstract][Full Text] [Related]
4. The occurrence of various non-delta F508 CFTR gene mutations among Hungarian cystic fibrosis patients. Nemeti M; Johnson JP; Papp Z; Louie E Hum Genet; 1992 May; 89(2):245-6. PubMed ID: 1375186 [TBL] [Abstract][Full Text] [Related]
5. Methods for analysis of multiple cystic fibrosis mutations. Ng IS; Pace R; Richard MV; Kobayashi K; Kerem B; Tsui LC; Beaudet AL Hum Genet; 1991 Sep; 87(5):613-7. PubMed ID: 1916764 [TBL] [Abstract][Full Text] [Related]
6. The incidence of different cystic fibrosis mutations in the Scottish population: effects on prenatal diagnosis and genetic counselling. Shrimpton AE; McIntosh I; Brock DJ J Med Genet; 1991 May; 28(5):317-21. PubMed ID: 1713973 [TBL] [Abstract][Full Text] [Related]
7. Genetic determination of exocrine pancreatic function in cystic fibrosis. Kristidis P; Bozon D; Corey M; Markiewicz D; Rommens J; Tsui LC; Durie P Am J Hum Genet; 1992 Jun; 50(6):1178-84. PubMed ID: 1376016 [TBL] [Abstract][Full Text] [Related]
8. Frequencies of cystic fibrosis mutations in the Maine population: high proportion of unknown alleles in individuals of French-Canadian ancestry. Bayleran JK; Yan H; Hopper CA; Simpson EM Hum Genet; 1996 Aug; 98(2):207-9. PubMed ID: 8698344 [TBL] [Abstract][Full Text] [Related]
9. Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene. Dörk T; Wulbrand U; Richter T; Neumann T; Wolfes H; Wulf B; Maass G; Tümmler B Hum Genet; 1991 Aug; 87(4):441-6. PubMed ID: 1715308 [TBL] [Abstract][Full Text] [Related]
10. Spectrum of CFTR mutations in Argentine cystic fibrosis patients. Chertkoff L; Visich A; Bienvenu T; Grenoville M; Segal E; Carniglia L; Kaplan JC; Barreiro C Clin Genet; 1997 Jan; 51(1):43-7. PubMed ID: 9084934 [TBL] [Abstract][Full Text] [Related]
11. Screening for cystic fibrosis gene mutations by multiplex DNA amplification. Picci L; Anglani F; Scarpa M; Zacchello F Hum Genet; 1992 Mar; 88(5):552-6. PubMed ID: 1551658 [TBL] [Abstract][Full Text] [Related]
12. Mutation analysis in 600 French cystic fibrosis patients. Chevalier-Porst F; Bonardot AM; Gilly R; Chazalette JP; Mathieu M; Bozon D J Med Genet; 1994 Jul; 31(7):541-4. PubMed ID: 7525963 [TBL] [Abstract][Full Text] [Related]
13. Simultaneous detection of delta F508, G542X, N1303K and 1717-1G-->A mutations in cystic fibrosis by capillary electrophoresis in polymer networks. Gelfi C; Righetti PG; Magnani C; Cremonesi L; Ferrari M Clin Chim Acta; 1994 Sep; 229(1-2):181-9. PubMed ID: 7527312 [No Abstract] [Full Text] [Related]
14. Simultaneous detection of delta F508, G542X, N1303K, G551D, and 1717-1G-->A cystic fibrosis alleles by a multiplex DNA enzyme immunoassay. Sangiuolo F; Maceratesi P; Mesoraca A; Botta A; Cavicchini A; Novelli G; Dallapiccola B Int J Clin Lab Res; 1995; 25(3):142-5. PubMed ID: 8562976 [TBL] [Abstract][Full Text] [Related]
15. The spectrum of CFTR mutations in south-west German cystic fibrosis patients. Lindner M; Wolf A; Moh B; Steinbach P; Kleihauer E; Bartram CR; Kulozik AE Hum Genet; 1992 Nov; 90(3):267-9. PubMed ID: 1283148 [TBL] [Abstract][Full Text] [Related]
16. Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reaction. Fortina P; Conant R; Monokian G; Dotti G; Parrella T; Hitchcock W; Kant J; Scanlin T; Rappaport E; Schwartz E Hum Genet; 1992 Dec; 90(4):375-8. PubMed ID: 1282898 [TBL] [Abstract][Full Text] [Related]
17. Molecular and clinical findings in Austrian cystic fibrosis patients with mutations in exon 11 of the CFTR gene. Greil I; Wagner K; Eber E; Zach M; Rosenkranz W Wien Klin Wochenschr; 1995; 107(15):464-9. PubMed ID: 7545856 [TBL] [Abstract][Full Text] [Related]
18. Screening for five mutations detects 97% of cystic fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population. Abeliovich D; Lavon IP; Lerer I; Cohen T; Springer C; Avital A; Cutting GR Am J Hum Genet; 1992 Nov; 51(5):951-6. PubMed ID: 1384328 [TBL] [Abstract][Full Text] [Related]
19. Ethnic heterogeneity and cystic fibrosis transmembrane regulator (CFTR) mutation frequencies in Chicago-area CF families. Ober C; Lester LA; Mott C; Billstrand C; Lemke A; van der Ven K; Marcus S; Kraut J; Lloyd-Still J; Booth C Am J Hum Genet; 1992 Dec; 51(6):1344-8. PubMed ID: 1281385 [TBL] [Abstract][Full Text] [Related]
20. Analysis of 30 known cystic fibrosis mutations: 10 mutations account for 27% of non-delta F508 chromosomes in southern France. Claustres M; Desgeorges M; Kjellberg P; Tissot C; Demaille J Hum Genet; 1992 Dec; 90(4):464-6. PubMed ID: 1483707 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]