123 related articles for article (PubMed ID: 7519028)
1. Identification of the linkage of mutations causing cystic fibrosis to different alleles of a tetranucleotide repeat in intron 6a of the CFTR gene.
Potapova OYu ; Voronina OV; Gaitskhoki VS; Bogacheva EV; Uembitskaya TE; Kuprina EA; Kapranov NI; Berlin YuA ; Schwartz EI
Biochem Med Metab Biol; 1994 Apr; 51(2):185-7. PubMed ID: 7519028
[TBL] [Abstract][Full Text] [Related]
2. [Detection of frequent mutations of the CFTR gene in cystic fibrosis patients from Central Russia].
Petrova NV; Kapranov NI; Ginter EK
Genetika; 1997 Jan; 33(1):106-9. PubMed ID: 9162681
[TBL] [Abstract][Full Text] [Related]
3. Linkage disequilibrium between cystic fibrosis mutations and polymorphic 4-bp repeat within CFTR gene.
Gaitskhoki VS; Voronina OV; Potapova OYu ; Kirjukhina LV; Gembitskaya TE; Kapranov NI; Petrova NV; Khafizova ZA; Schwartz EI
Biochem Med Metab Biol; 1993 Oct; 50(2):186-9. PubMed ID: 7505092
[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. Study of 12 mutations in Turkish cystic fibrosis patients.
Yilmaz E; Erdem H; Ozgüç M; Coşkun T; Ozçelik U; Göçmen A; Ozalp I
Hum Hered; 1995; 45(3):175-7. PubMed ID: 7542223
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. 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]
9. [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]
10. 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]
11. CFTR gene: molecular analysis in patients from South Brazil.
Streit C; Burlamaque-Neto AC; de Abreu e Silva F; Giugliani R; Saraiva Pereira ML
Mol Genet Metab; 2003 Apr; 78(4):259-64. PubMed ID: 12706377
[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. Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutation.
Kanavakis E; Tzetis M; Antoniadi T; Traeger-Synodinos J; Doudounakis S; Adam G; Matsaniotis N; Kattamis C
Hum Genet; 1995 Sep; 96(3):364-6. PubMed ID: 7544320
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. [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]
17. A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
Zielenski J; Markiewicz D; Rininsland F; Rommens J; Tsui LC
Am J Hum Genet; 1991 Dec; 49(6):1256-62. PubMed ID: 1720926
[TBL] [Abstract][Full Text] [Related]
18. [Molecular-genetic analysis of certain mutations of the "cystic fibrosis gene" in Moldavia. Characteristics of molecular markers and their linkage with various mutations].
Gimbovskaia SD; Kalinin VN; Ivashchenko TE; Baranov VS
Genetika; 1994 Dec; 30(12):1616-20. PubMed ID: 7534245
[TBL] [Abstract][Full Text] [Related]
19. Rapid characterization of the variable length polythymidine tract in the cystic fibrosis (CFTR) gene: association of the 5T allele with selected CFTR mutations and its incidence in atypical sinopulmonary disease.
Friedman KJ; Heim RA; Knowles MR; Silverman LM
Hum Mutat; 1997; 10(2):108-15. PubMed ID: 9259194
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]