80 related articles for article (PubMed ID: 11216394)
1. Microsatellite haplotypes associations with 5 CFTR mutations in "Grande Brière", an isolate located in southern Brittany.
Bezieau S; Picherot G; David A; De Braekeleer M; Ferec C; Moisan JP; Chaventré A
Coll Antropol; 2000 Dec; 24(2):281-6. PubMed ID: 11216394
[TBL] [Abstract][Full Text] [Related]
2. Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis.
Moutou C; Gardes N; Viville S
Eur J Hum Genet; 2002 Apr; 10(4):231-8. PubMed ID: 12032730
[TBL] [Abstract][Full Text] [Related]
3. [Characterization of 3 microsatellites of the cystic fibrosis gene in Argentine families].
Visich AA; Barreiro CZ; Chertkoff LP
Medicina (B Aires); 2001; 61(1):23-7. PubMed ID: 11265619
[TBL] [Abstract][Full Text] [Related]
4. Polymorphic markers suggest a gene flow of CFTR gene from Sub-Saharan/Arabian and Mediterranean to Brazilian Population.
Cabello GM; Cabello PH; Llerena JC; Fernandes O
J Hered; 2006; 97(4):313-7. PubMed ID: 16837565
[TBL] [Abstract][Full Text] [Related]
5. Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles.
Faucz FR; Gimenez J; Ramos MD; Pereira-Ferrari L; Estivill X; Raskin S; Casals T; Culpi L
Clin Genet; 2007 Sep; 72(3):218-23. PubMed ID: 17718859
[TBL] [Abstract][Full Text] [Related]
6. Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960.
Scotet V; Gillet D; Duguépéroux I; Audrézet MP; Bellis G; Garnier B; Roussey M; Rault G; Parent P; De Braekeleer M; Férec C;
Hum Genet; 2002 Sep; 111(3):247-54. PubMed ID: 12215837
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population.
Russo MP; Romeo G; Devoto M; Barbujani G; Cabrini G; Giunta A; D'Alcamo E; Leoni G; Sangiuolo F; Magnani C
Hum Mutat; 1995; 5(1):23-7. PubMed ID: 7537148
[TBL] [Abstract][Full Text] [Related]
9. Mutational spectrum of cystic fibrosis patients from Córdoba province and its zone of influence: implications of molecular diagnosis in Argentina.
Ramírez AM; Ramos MD; Jiménez J; Ghio A; de Botelli MM; Rezzónico CA; Marqués I; Pereyro S; Casals T; de Kremer RD
Mol Genet Metab; 2006 Apr; 87(4):370-5. PubMed ID: 16423550
[TBL] [Abstract][Full Text] [Related]
10. CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern France.
Claustres M; Desgeorges M; Moine P; Morral N; Estivill X
Hum Genet; 1996 Sep; 98(3):336-44. PubMed ID: 8707306
[TBL] [Abstract][Full Text] [Related]
11. [Analysis of the spectra of mutations and polymorphic loci of cystic fibrosis transmembrane conductance regulator in the population of Bashkortostan].
Korytina GF; Viktorova TV; Baĭkova GV; Khusnutdinova EK
Genetika; 2002 Sep; 38(9):1270-5. PubMed ID: 12391889
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases.
Lee JH; Choi JH; Namkung W; Hanrahan JW; Chang J; Song SY; Park SW; Kim DS; Yoon JH; Suh Y; Jang IJ; Nam JH; Kim SJ; Cho MO; Lee JE; Kim KH; Lee MG
Hum Mol Genet; 2003 Sep; 12(18):2321-32. PubMed ID: 12952861
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Comparison of the CFTR mutation spectrum in three cohorts of patients of Celtic origin from Brittany (France) and Ireland.
Scotet V; Barton DE; Watson JB; Audrézet MP; McDevitt T; McQuaid S; Shortt C; De Braekeleer M; Férec C; Le Maréchal C
Hum Mutat; 2003 Jul; 22(1):105. PubMed ID: 12815607
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations.
Kinnunen S; Bonache S; Casals T; Monto S; Savilahti E; Kere J; Järvelä I
J Cyst Fibros; 2005 Dec; 4(4):233-7. PubMed ID: 16051530
[TBL] [Abstract][Full Text] [Related]
17. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
Schwartz M
Ugeskr Laeger; 2003 Feb; 165(9):912-6. PubMed ID: 12661515
[TBL] [Abstract][Full Text] [Related]
18. Instability of the insertional mutation in CftrTgH(neoim)Hgu cystic fibrosis mouse model.
Charizopoulou N; Jansen S; Dorsch M; Stanke F; Dorin JR; Hedrich HJ; Tümmler B
BMC Genet; 2004 Apr; 5():6. PubMed ID: 15102331
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of intragenic polymorphic markers of the CFTR gene in cystic fibrosis patients and health donors from Bashkorostan].
Korytina GF; Viktorova TV; Uvashchenko TE; Baranov VS; Khusnutdinova EK
Genetika; 2003 Nov; 39(11):1542-9. PubMed ID: 14714468
[TBL] [Abstract][Full Text] [Related]
20. Immunoreactive trypsin/DNA newborn screening for cystic fibrosis: should the R117H variant be included in CFTR mutation panels?
Scotet V; Audrézet MP; Roussey M; Rault G; Dirou-Prigent A; Journel H; Moisan-Petit V; Storni V; Férec C
Pediatrics; 2006 Nov; 118(5):e1523-9. PubMed ID: 17015492
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
