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Journal Abstract Search

283 related items for PubMed ID: 1715311

  • 1. Molecular analysis of cystic fibrosis in the Hungarian population.
    Nemeti M, Louie E, Papp Z, Johnson JP.
    Hum Genet; 1991 Aug; 87(4):511-2. PubMed ID: 1715311
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  • 2. 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
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  • 4. Deletion delta F508 and haplotype analysis of CFTR gene region in Slovak CF patients.
    Kádasi L, Gécz J, Matúsek J, Krivusová T, Ferák V, Devoto M, Hruskovic J, Romeo G.
    Hum Genet; 1992 May; 89(3):305-6. PubMed ID: 1376297
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  • 5. Cystic fibrosis gene mutations and linked RFLPs in the Slovenian population.
    Ravnik-Glavac M, Gasparini P, Peterlin B, Strukelj M, Glavac D, Canki-Klain N, Pignatti PF, Komel R.
    Ann Genet; 1992 May; 35(2):85-8. PubMed ID: 1355957
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  • 7. The occurrence of various non-delta F508 CFTR gene mutations among Hungarian cystic fibrosis patients.
    Nemeti M, Johnson JP, Papp Z, Louie E.
    Hum Genet; 1992 May; 89(2):245-6. PubMed ID: 1375186
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  • 8. Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population.
    Vidaud M, Kitzis A, Ferec C, Bozon D, Dumur V, Giraud G, David F, Pascal O, Auvinet M, Morel Y.
    Hum Genet; 1989 Jan; 81(2):183-4. PubMed ID: 2563252
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  • 10. 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
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  • 12. Frequency of the delta F508 and exon 11 mutations in Norwegian cystic fibrosis patients.
    Eiklid K, Tranebjaerg L, Eiken HG, Pedersen JC, Michalsen H, Fluge G, Schwartz M, Nilsen BR, Bolle R, Skyberg D.
    Clin Genet; 1993 Jul; 44(1):12-4. PubMed ID: 7691448
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  • 15. 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
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  • 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
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  • 20. Allele frequencies of cystic fibrosis-linked markers and F508 deletion in affected Hungarian families.
    Endreffy E, Burg K, Gyurkovits K, Kálmán M, László A, Raskó I.
    Acta Paediatr Hung; 1992 Sep; 32(2):101-13. PubMed ID: 1356379
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