170 related articles for article (PubMed ID: 14714468)
1. [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]
2. [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]
3. [Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region].
Sazonova MA; Amosenko FA; Kapranov NI; Kalinin VN
Genetika; 1997 Sep; 33(9):1303-7. PubMed ID: 9445824
[TBL] [Abstract][Full Text] [Related]
4. [Portion of certain cystic fibrosis gene mutations and linkage dysequilibrium between the CFTR-gene locus and two DNA marker loci in Russian populations].
Petrova NV; Ginter EK; Kapranov NI; El'chinova GI
Genetika; 1994 Jul; 30(7):974-7. PubMed ID: 7525404
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [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]
7. [Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region].
Amosenko FA; Sazonova MA; Kapranov NI; Trubnikova IS; Kalinin VN
Genetika; 1995 Apr; 31(4):532-5. PubMed ID: 7607440
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. [An analysis of the mutations in the mucoviscidosis gene: the origin and distribution of the delF508 major mutation in Ukraine].
Livshits LA; Kravchenko SA; Musienko SI; Maliarchuk SG
Tsitol Genet; 1995; 29(6):67-73. PubMed ID: 8713839
[TBL] [Abstract][Full Text] [Related]
11. Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation.
Cuppens H; Lin W; Jaspers M; Costes B; Teng H; Vankeerberghen A; Jorissen M; Droogmans G; Reynaert I; Goossens M; Nilius B; Cassiman JJ
J Clin Invest; 1998 Jan; 101(2):487-96. PubMed ID: 9435322
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. [Mutation p.E92K is the primary cause of cystic fibrosis in Chuvashes].
Stepanova AA; Abrukova AV; Savaskina EN; Poliakov AV
Genetika; 2012 Jul; 48(7):863-71. PubMed ID: 22988772
[TBL] [Abstract][Full Text] [Related]
17. The cradle of the deltaF508 mutation.
Saleheen D; Frossard PM
J Ayub Med Coll Abbottabad; 2008; 20(4):157-60. PubMed ID: 19999232
[TBL] [Abstract][Full Text] [Related]
18. Identification and characterization of CFTR gene mutations in Indian CF patients.
Sharma N; Singh M; Kaur G; Thapa BR; Prasad R
Ann Hum Genet; 2009 Jan; 73(1):26-33. PubMed ID: 18782298
[TBL] [Abstract][Full Text] [Related]
19. Microsatellite haplotypes of Polish cystic fibrosis alleles: delta F508 chromosomes demonstrate a North-South haplotype frequency gradient.
Witt M; Reis A; Cichy W; Dziechciowska K
Hum Hered; 1996; 46(6):310-4. PubMed ID: 8956026
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
