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165 related items for PubMed ID: 2037283
1. Frequency of the F508 deletion in cystic fibrosis patients from the European part of the USSR. Baranov VS, Ivaschenko TE, Gorbunova VN, Livshitz LA, Venozinskis MT, Gembovskaya SA, Kalinin VN, Romanenko OP, Gembitzkaya TE, Orlov AV. Hum Genet; 1991 May; 87(1):61-4. PubMed ID: 2037283 [Abstract] [Full Text] [Related]
4. 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 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
8. 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 Sep; 45(1):55-7. PubMed ID: 7896301 [Abstract] [Full Text] [Related]
9. Gradient of distribution in Europe of the major CF mutation and of its associated haplotype. European Working Group on CF Genetics (EWGCFG). Hum Genet; 1990 Sep; 85(4):436-45. PubMed ID: 2210767 [Abstract] [Full Text] [Related]
10. Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patients. Wauters JG, Hendrickx J, Coucke P, Vits L, Stuer K, van Schil L, van der Auwera BJ, Van Elsen A, Dumon J, Willems PJ. Clin Genet; 1991 Feb; 39(2):89-92. PubMed ID: 1673094 [Abstract] [Full Text] [Related]
11. Cystic fibrosis in the Basque country: high frequency of mutation delta F508 in patients of Basque origin. Casals T, Vázquez C, Lázaro C, Girbau E, Giménez FJ, Estivill X. Am J Hum Genet; 1992 Feb; 50(2):404-10. PubMed ID: 1370875 [Abstract] [Full Text] [Related]
12. 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 [Abstract] [Full Text] [Related]
13. delta F508 frequency and associated haplotypes near the cystic fibrosis locus in the Yugoslav population. Simova L, Williams C, Efremov GD, Gordova-Muratovska A, Sustić S, Watson EK, Williamson R. Hum Genet; 1990 Sep; 85(4):432-3. PubMed ID: 1976597 [Abstract] [Full Text] [Related]
14. Distribution of the delta F508 mutation in 194 Spanish cystic fibrosis families. Chillón M, Nunes V, Casals T, Giménez FJ, Fernández E, Benítez J, Estivill X. Hum Genet; 1990 Sep; 85(4):396-7. PubMed ID: 2210743 [Abstract] [Full Text] [Related]
15. Molecular data on cystic fibrosis in Bulgaria. Kalaydjieva L, Antov J, Bronzova J, Vladimirova V, Horst J. Hum Genet; 1990 Sep; 85(4):412-3. PubMed ID: 1976594 [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 [Abstract] [Full Text] [Related]
17. 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 [Abstract] [Full Text] [Related]
19. [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 [Abstract] [Full Text] [Related]