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2. Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins. Tishkoff SA; Pakstis AJ; Stoneking M; Kidd JR; Destro-Bisol G; Sanjantila A; Lu RB; Deinard AS; Sirugo G; Jenkins T; Kidd KK; Clark AG Am J Hum Genet; 2000 Oct; 67(4):901-25. PubMed ID: 10986042 [TBL] [Abstract][Full Text] [Related]
3. PKLR- GBA region shows almost complete linkage disequilibrium over 70 kb in a set of worldwide populations. Mateu E; Pérez-Lezaun A; Martínez-Arias R; Andrés A; Vallés M; Bertranpetit J; Calafell F Hum Genet; 2002 Jun; 110(6):532-44. PubMed ID: 12107439 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Global survey of haplotype frequencies and linkage disequilibrium at the RET locus. Chattopadhyay P; Pakstis AJ; Mukherjee N; Iyengar S; Odunsi A; Okonofua F; Bonne-Tamir B; Speed W; Kidd JR; Kidd KK Eur J Hum Genet; 2003 Oct; 11(10):760-9. PubMed ID: 14512966 [TBL] [Abstract][Full Text] [Related]
6. Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations. Nakajima T; Jorde LB; Ishigami T; Umemura S; Emi M; Lalouel JM; Inoue I Am J Hum Genet; 2002 Jan; 70(1):108-23. PubMed ID: 11731937 [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. A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus. Kidd KK; Morar B; Castiglione CM; Zhao H; Pakstis AJ; Speed WC; Bonne-Tamir B; Lu RB; Goldman D; Lee C; Nam YS; Grandy DK; Jenkins T; Kidd JR Hum Genet; 1998 Aug; 103(2):211-27. PubMed ID: 9760208 [TBL] [Abstract][Full Text] [Related]
10. Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations. Kidd JR; Pakstis AJ; Zhao H; Lu RB; Okonofua FE; Odunsi A; Grigorenko E; Tamir BB; Friedlaender J; Schulz LO; Parnas J; Kidd KK Am J Hum Genet; 2000 Jun; 66(6):1882-99. PubMed ID: 10788337 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of Brittany. De Braekeleer M; Chaventré A; Bertorelle G; Verlingue C; Raguénès O; Mercier B; Férec C Hum Genet; 1996 Aug; 98(2):223-7. PubMed ID: 8698348 [TBL] [Abstract][Full Text] [Related]
13. [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]
14. 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]
15. CFTR haplotype backgrounds on normal and mutant CFTR genes. Cuppens H; Teng H; Raeymaekers P; De Boeck C; Cassiman JJ Hum Mol Genet; 1994 Apr; 3(4):607-14. PubMed ID: 7520797 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretion. Stanke F; Hedtfeld S; Becker T; Tümmler B BMC Med Genet; 2011 May; 12():62. PubMed ID: 21548936 [TBL] [Abstract][Full Text] [Related]
19. Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations. Pompei F; Ciminelli BM; Bombieri C; Ciccacci C; Koudova M; Giorgi S; Belpinati F; Begnini A; Cerny M; Des Georges M; Claustres M; Ferec C; Macek M; Modiano G; Pignatti PF Eur J Hum Genet; 2006 Jan; 14(1):85-93. PubMed ID: 16251901 [TBL] [Abstract][Full Text] [Related]
20. Lactase haplotype diversity in the Old World. Hollox EJ; Poulter M; Zvarik M; Ferak V; Krause A; Jenkins T; Saha N; Kozlov AI; Swallow DM Am J Hum Genet; 2001 Jan; 68(1):160-172. PubMed ID: 11095994 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]