182 related articles for article (PubMed ID: 9012419)
1. Estimating the age of alleles by use of intraallelic variability.
Slatkin M; Rannala B
Am J Hum Genet; 1997 Feb; 60(2):447-58. PubMed ID: 9012419
[TBL] [Abstract][Full Text] [Related]
2. The use of intraallelic variability for testing neutrality and estimating population growth rate.
Slatkin M; Bertorelle G
Genetics; 2001 Jun; 158(2):865-74. PubMed ID: 11404347
[TBL] [Abstract][Full Text] [Related]
3. Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens.
Ravnik-Glavac M; Dean M; Glavac D
Pflugers Arch; 2000; 439(3 Suppl):R53-5. PubMed ID: 10653141
[TBL] [Abstract][Full Text] [Related]
4. Application of multiplex ARMS and SSCP/HD analysis in molecular diagnosis of cystic fibrosis in Indian patients.
Ashavaid TF; Kondkar AA; Dherai AJ; Raghavan R; Udani SV; Udwadia ZF; Desai D
Mol Diagn; 2005; 9(2):59-66. PubMed ID: 16137181
[TBL] [Abstract][Full Text] [Related]
5. Isolation of CF cell lines corrected at DeltaF508-CFTR locus by SFHR-mediated targeting.
Bruscia E; Sangiuolo F; Sinibaldi P; Goncz KK; Novelli G; Gruenert DC
Gene Ther; 2002 Jun; 9(11):683-5. PubMed ID: 12032687
[TBL] [Abstract][Full Text] [Related]
6. A vectorized method of importance sampling with applications to models of mutation and migration.
Slatkin M
Theor Popul Biol; 2002 Dec; 62(4):339-48. PubMed ID: 12427457
[TBL] [Abstract][Full Text] [Related]
7. Cystic fibrosis transmembrane regulator (CFTR) DeltaF508 mutation and 5T allele in patients with chronic pancreatitis and exocrine pancreatic cancer. PANKRAS II Study Group.
Malats N; Casals T; Porta M; Guarner L; Estivill X; Real FX
Gut; 2001 Jan; 48(1):70-4. PubMed ID: 11115825
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. 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]
10. The 3120 +1G-->A splicing mutation in CFTR is common in Brazilian cystic fibrosis patients.
Cabello GM; Cabello EH JL; Fernande O; Harris A
Hum Biol; 2001 Jun; 73(3):403-9. PubMed ID: 11459421
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Analysis of cystic fibrosis gene mutations and associated haplotypes in the Croatian population.
Knezević J; Tanacković G; Matijević T; Barisić I; Pavelić J
Genet Test; 2007; 11(2):133-8. PubMed ID: 17627383
[TBL] [Abstract][Full Text] [Related]
13. Molecular analysis of 23 exons of the CFTR gene in Brazilian patients leads to the finding of rare cystic fibrosis mutations.
Cabello GM; Cabello PH; Otsuki K; Gombarovits ME; Llerena JC; Fernandes O
Hum Biol; 2005 Feb; 77(1):125-35. PubMed ID: 16114821
[TBL] [Abstract][Full Text] [Related]
14. Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.
Sharma H; Mavuduru RS; Singh SK; Prasad R
Mol Hum Reprod; 2014 Sep; 20(9):827-35. PubMed ID: 24958810
[TBL] [Abstract][Full Text] [Related]
15. CFTR mutations in three Latin American countries.
Restrepo CM; Pineda L; Rojas-Martínez A; Gutiérrez CA; Morales A; Gómez Y; Villalobos MC; Borjas L; Delgado W; Myers A; Barrera-Saldaña HA
Am J Med Genet; 2000 Apr; 91(4):277-9. PubMed ID: 10766983
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.
Dörk T; Macek M; Mekus F; Tümmler B; Tzountzouris J; Casals T; Krebsová A; Koudová M; Sakmaryová I; Macek M; Vávrová V; Zemková D; Ginter E; Petrova NV; Ivaschenko T; Baranov V; Witt M; Pogorzelski A; Bal J; Zékanowsky C; Wagner K; Stuhrmann M; Bauer I; Seydewitz HH; Neumann T; Jakubiczka S
Hum Genet; 2000 Mar; 106(3):259-68. PubMed ID: 10798353
[TBL] [Abstract][Full Text] [Related]
17. Polymorphism of cystic fibrosis gene in Japanese patients with chronic pancreatitis.
Kimura S; Okabayashi Y; Inushima K; Yutsudo Y; Kasuga M
Dig Dis Sci; 2000 Oct; 45(10):2007-12. PubMed ID: 11117575
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mutation analysis of CFTR gene in 70 Iranian cystic fibrosis patients.
Alibakhshi R; Zamani M
Iran J Allergy Asthma Immunol; 2006 Mar; 5(1):3-8. PubMed ID: 17242497
[TBL] [Abstract][Full Text] [Related]
20. Can a place of origin of the main cystic fibrosis mutations be identified?
Mateu E; Calafell F; Ramos MD; Casals T; Bertranpetit J
Am J Hum Genet; 2002 Jan; 70(1):257-64. PubMed ID: 11713719
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
