130 related articles for article (PubMed ID: 11484207)
1. XV-2c/KM-19 haplotype analysis of cystic fibrosis mutations in Mexican patients.
Orozco L; González L; Chávez M; Velázquez R; Lezana JL; Saldaña Y; Villarreal T; Carnevale A
Am J Med Genet; 2001 Aug; 102(3):277-81. PubMed ID: 11484207
[TBL] [Abstract][Full Text] [Related]
2. XV-2c/KM19 haplotypes analysis of cystic fibrosis patients from western Mexico.
Flores-Martínez SE; Martínez JF; Machorro-Lazo MV; García-Zapién AG; Salgado-Goytia L; Cruz-Quevedo EG; Morán-Moguel MC; Sánchez-Corona J
Acta Physiol Hung; 2008 Sep; 95(3):313-25. PubMed ID: 18788470
[TBL] [Abstract][Full Text] [Related]
3. Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis.
Sereth H; Shoshani T; Bashan N; Kerem BS
Hum Genet; 1993 Oct; 92(3):289-95. PubMed ID: 7691712
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Molecular basis of cystic fibrosis in the Republic of Macedonia.
Petreska L; Koceva S; Plaseska D; Chernick M; Gordova-Muratovska A; Fustic S; Nestorov R; Efremov GD
Clin Genet; 1998 Sep; 54(3):203-9. PubMed ID: 9788722
[TBL] [Abstract][Full Text] [Related]
6. Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.
Morral N; Nunes V; Casals T; Chillón M; Giménez J; Bertranpetit J; Estivill X
Hum Mol Genet; 1993 Jul; 2(7):1015-22. PubMed ID: 7689896
[TBL] [Abstract][Full Text] [Related]
7. Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers.
Morral N; Dörk T; Llevadot R; Dziadek V; Mercier B; Férec C; Costes B; Girodon E; Zielenski J; Tsui LC; Tümmler B; Estivill X
Hum Mutat; 1996; 8(2):149-59. PubMed ID: 8844213
[TBL] [Abstract][Full Text] [Related]
8. Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients.
Simon-Bouy B; Mornet E; Serre JL; Taillandier A; Boué J; Boué A
Clin Genet; 1991 Sep; 40(3):218-24. PubMed ID: 1723032
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis in a cystic fibrosis family: a combined molecular strategy for a precise diagnosis.
Chávez-Saldaña M; García-Cavazos R; Vigueras RM; Orozco L
Rev Invest Clin; 2011; 63(4):433-5. PubMed ID: 22364044
[TBL] [Abstract][Full Text] [Related]
10. Haplotype analysis of the CFTR gene on normal and mutant CFTR genes.
Karimi N; Bidemeshki Pour A; Alibakhshi R; Almasi S
Mutat Res; 2020; 821():111708. PubMed ID: 32563932
[TBL] [Abstract][Full Text] [Related]
11. Mutation analysis and haplotype correlation for 139 cystic fibrosis patients from the Nebraska Regional Cystic Fibrosis Center.
Traystman MD; Schulte N; Colombo JL; Sammut PH; Reilly P; Patel C; Acquazzino D; Simanek B; Anderson R; Kimberling WJ
Hum Mutat; 1993; 2(1):7-15. PubMed ID: 7682884
[TBL] [Abstract][Full Text] [Related]
12. XV-2c and KM.19 haplotype analysis in Chilean patients with cystic fibrosis and unknown CFTR gene mutations.
Repetto GM; Puga AR; Delgado I
Biol Res; 2007; 40(2):223-9. PubMed ID: 18064359
[TBL] [Abstract][Full Text] [Related]
13. Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.
Dörk T; Neumann T; Wulbrand U; Wulf B; Kälin N; Maass G; Krawczak M; Guillermit H; Ferec C; Horn G
Hum Genet; 1992 Feb; 88(4):417-25. PubMed ID: 1371263
[TBL] [Abstract][Full Text] [Related]
14. Cystic fibrosis mutations and associated haplotypes in Bulgaria - a comparative population genetic study.
Angelicheva D; Calafell F; Savov A; Jordanova A; Kufardjieva A; Galeva I; Nedkova V; Ivanova T; Yankova P; Konstantinova D; Genev E; Kalaydjieva L
Hum Genet; 1997 Apr; 99(4):513-20. PubMed ID: 9099843
[TBL] [Abstract][Full Text] [Related]
15. Association between haplotypes and specific mutations in Swiss cystic fibrosis families.
Liechti-Gallati S; Malik N; Alkan M; Maechler M; Morris M; Thonney F; Sennhauser F; Moser H
Pediatr Res; 1991 Oct; 30(4):304-8. PubMed ID: 1683481
[TBL] [Abstract][Full Text] [Related]
16. Haplotype distribution of and linkage disequilibrium between four polymorphic markers near the CFTR locus in Brazilian cystic fibrosis patients.
Cabello GM; Cabello PH; Lopez-Camelo JS; Llerena JC; Fernandes O
Hum Biol; 2005 Dec; 77(6):853-65. PubMed ID: 16715841
[TBL] [Abstract][Full Text] [Related]
17. A haplotype framework for cystic fibrosis mutations in Iran.
Elahi E; Khodadad A; Kupershmidt I; Ghasemi F; Alinasab B; Naghizadeh R; Eason RG; Amini M; Esmaili M; Esmaeili Dooki MR; Sanati MH; Davis RW; Ronaghi M; Thorstenson YR
J Mol Diagn; 2006 Feb; 8(1):119-27. PubMed ID: 16436643
[TBL] [Abstract][Full Text] [Related]
18. Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomes.
Hughes D; Wallace A; Taylor J; Tassabehji M; McMahon R; Hill A; Nevin N; Graham C
Hum Mutat; 1996; 8(3):229-35. PubMed ID: 8889582
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Cystic fibrosis gene variability in two southern Brazilian Amerindian populations: analysis of the deltaF508 mutation and the KM19 and XV2C haplotypes.
Raskin S; Petzl-Erler ML; Phillips JA; Pereira-Ferrari L; Probst CM; Faucz FR; Sotomaior V; Salzano FM; Culpi L
Hum Biol; 2007 Feb; 79(1):79-91. PubMed ID: 17985657
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
