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.
165 related articles for article (PubMed ID: 1990833)
1. A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation origin. Chehab FF; Johnson J; Louie E; Goossens M; Kawasaki E; Erlich H Am J Hum Genet; 1991 Feb; 48(2):223-6. PubMed ID: 1990833 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Frequency of delta-F508 mutation and XV2C/KM19 haplotypes in Cuban cystic fibrosis families. Collazo T; Magarino C; Chavez R; Suardiaz B; Gispert S; Gomez M; Rojo M; Heredero L Hum Hered; 1995; 45(1):55-7. PubMed ID: 7896301 [TBL] [Abstract][Full Text] [Related]
6. Frequency of the delta F508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without delta F508 still in disequilibrium. Scheffer H; Bruinvels DJ; te Meerman GJ; Verlind E; Penninga D; Dankert J; Ten Kate LP; Buys CH Hum Genet; 1990 Sep; 85(4):425-7. PubMed ID: 2210761 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Analysis of CA/GT microsatellite polymorphism in IVS8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a study of Italian CF families. Restagno G; Garnerone S; Gennaro C; Ferrone M; Carbonara A Clin Genet; 1992 Dec; 42(6):309-13. PubMed ID: 1283566 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. [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]
11. Cystic fibrosis typing with DNA probes and screening for delta F508 deletion in families from southern France. Claustres M; Desgeorges M; Kjellberg P; Bellet H; Demaille J; Ramsay M Hum Genet; 1990 Sep; 85(4):398-9. PubMed ID: 1976591 [TBL] [Abstract][Full Text] [Related]
12. The haplotype distribution of the delta F508 mutation in cystic fibrosis families in Scotland. McIntosh I; Curtis A; Lorenzo ML; Keston M; Gilfillan AJ; Morris G; Brock DJ Hum Genet; 1990 Sep; 85(4):419-20. PubMed ID: 2210756 [TBL] [Abstract][Full Text] [Related]
13. [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]
14. The incidence of delta F508 CF mutation, and associated haplotypes, in a sample of English CF families. Watson EK; Mayall ES; Simova L; Thompson EM; Warner JO; Williamson R; Williams C Hum Genet; 1990 Sep; 85(4):435-6. PubMed ID: 2210766 [TBL] [Abstract][Full Text] [Related]
15. [Screening of the delta-F508 mutation and analysis of two Single Nucleotide Polymorphism of the CFTR gene, in a sample of the general population of Valparaíso, Chile]. Vera A; Henríquez-Roldán CF; González FJ; Molina G Rev Med Chil; 2005 Jul; 133(7):767-75. PubMed ID: 16341382 [TBL] [Abstract][Full Text] [Related]
16. Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian families. Cuppens H; Legius E; Cabello P; Marynen P; De Boeck C; Decorte R; Fryns JP; Eggermont E; Van den Berghe H; Cassiman JJ Hum Genet; 1990 Sep; 85(4):402-3. PubMed ID: 2210747 [TBL] [Abstract][Full Text] [Related]
17. The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and Arabs. Lerer I; Cohen S; Chemke M; Sanilevich A; Rivlin J; Golan A; Yahav J; Friedman A; Abeliovich D Hum Genet; 1990 Sep; 85(4):416-7. PubMed ID: 1976595 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. delta F508 deletion in cystic fibrosis in Italian families. Restagno G; Garnerone S; Gennaro C; Varetto O; Ansaldi N; Castello D; Santini B; Carbonara AO Hum Genet; 1990 Sep; 85(4):422-3. PubMed ID: 1976596 [TBL] [Abstract][Full Text] [Related]
20. Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations. Dörk T; Fislage R; Neumann T; Wulf B; Tümmler B Hum Genet; 1994 Jan; 93(1):67-73. PubMed ID: 7505767 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]