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24. Association between haplotypes and specific mutations in Swiss cystic fibrosis families. Liechti-Gallati S; Malik N; Alkan M; Maechler M; Morris M; Thonney F; Sennhauser F; Moser H Pediatr Res; 1991 Oct; 30(4):304-8. PubMed ID: 1683481 [TBL] [Abstract][Full Text] [Related]
25. Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP. Estivill X; McLean C; Nunes V; Casals T; Gallano P; Scambler P; Williamson R Am J Hum Genet; 1989 May; 44(5):704-10. PubMed ID: 2565082 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. Genetic differences between cystic fibrosis with and without meconium ileus. Mornet E; Simon-Bouy B; Serre JL; Estivill X; Farrall M; Williamson R; Boue J; Boue A Lancet; 1988 Feb; 1(8582):376-8. PubMed ID: 2893188 [TBL] [Abstract][Full Text] [Related]
28. Lung involvement, the delta F508 mutation and DNA haplotype analysis in cystic fibrosis. Santamaria F; Salvatore D; Castiglione O; Raia V; de Ritis G; Sebastio G Hum Genet; 1992 Mar; 88(6):639-41. PubMed ID: 1348048 [TBL] [Abstract][Full Text] [Related]
29. Correlation of phenotypic and genetic heterogeneity in cystic fibrosis: variability in sweat electrolyte levels contributes to heterogeneity and is increased with the XV-2c/KM19 B haplotype. Witt M; Erickson RP; Ober C; Howatt WF; Farber R Am J Med Genet; 1991 May; 39(2):137-43. PubMed ID: 2063915 [TBL] [Abstract][Full Text] [Related]
30. The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosis. Gasparini P; Novelli G; Estivill X; Olivieri D; Savoia A; Ruzzo A; Nunes V; Borgo G; Antonelli M; Williamson R J Med Genet; 1990 Jan; 27(1):17-20. PubMed ID: 1968514 [TBL] [Abstract][Full Text] [Related]
31. Mutation analysis and haplotype correlation for 139 cystic fibrosis patients from the Nebraska Regional Cystic Fibrosis Center. Traystman MD; Schulte N; Colombo JL; Sammut PH; Reilly P; Patel C; Acquazzino D; Simanek B; Anderson R; Kimberling WJ Hum Mutat; 1993; 2(1):7-15. PubMed ID: 7682884 [TBL] [Abstract][Full Text] [Related]
32. Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. Beaudet A; Bowcock A; Buchwald M; Cavalli-Sforza L; Farrall M; King MC; Klinger K; Lalouel JM; Lathrop G; Naylor S Am J Hum Genet; 1986 Dec; 39(6):681-93. PubMed ID: 3026171 [TBL] [Abstract][Full Text] [Related]
33. Polymorphic DNA markers linked to cystic fibrosis locus in 20 Italian nuclear families. Novelli G; Potenza L; Ruzzo A; Dallapiccola B Gene Geogr; 1987 Dec; 1(3):193-9. PubMed ID: 3154126 [TBL] [Abstract][Full Text] [Related]
34. Frequency of delta F508 and haplotype association in Austrian cystic fibrosis families. Wagner K; Zach M; Rosenkranz W Hum Genet; 1992 Jun; 89(4):437-8. PubMed ID: 1377659 [TBL] [Abstract][Full Text] [Related]
35. Three additional DNA polymorphisms in the met gene and D7S8 locus: use in prenatal diagnosis of cystic fibrosis. Dean M; O'Connell P; Leppert M; Park M; Amos JA; Phillips DG; White R; Vande Woude GF J Pediatr; 1987 Oct; 111(4):490-5. PubMed ID: 2888841 [TBL] [Abstract][Full Text] [Related]
36. [Genetic study in 8 families with a child with cystic fibrosis]. Riedler J; Arrer E; Grabherr B Wien Klin Wochenschr; 1989 Sep; 101(16):548-51. PubMed ID: 2572089 [TBL] [Abstract][Full Text] [Related]