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Journal Abstract Search

188 related items for PubMed ID: 1356071

  • 1. [The delta F508 mutation which causes cystic fibrosis and its association with closely linked DNA polymorphisms in the Slovak population].
    Kádasi L, Gécz J, Puliti A, Devoto M, Ferák V, Romeo G, Kayserová H, Kardosová A, Hruskovic I.
    Bratisl Lek Listy; 1992 Mar; 93(3):141-5. PubMed ID: 1356071
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  • 2. 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 Mar; 35(2):85-8. PubMed ID: 1355957
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  • 3. 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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  • 4. 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
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  • 5. 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
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  • 6. Genotyping of the Spanish cystic fibrosis population at the delta F508 mutation site and RFLP linked loci.
    Jaume-Roig B, Simon-Bouy B, Taillandier A, Serre JL, Antich J, Bellon J, Boué J, Boué A.
    Hum Genet; 1990 Sep; 85(4):410-1. PubMed ID: 1976593
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  • 7. Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis.
    Sereth H, Shoshani T, Bashan N, Kerem BS.
    Hum Genet; 1993 Oct 01; 92(3):289-95. PubMed ID: 7691712
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  • 8. 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 01; 85(4):398-9. PubMed ID: 1976591
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  • 15. 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 01; 32(2):101-13. PubMed ID: 1356379
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  • 16. 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 01; 85(4):425-7. PubMed ID: 2210761
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  • 18. Molecular analysis of cystic fibrosis in the Hungarian population.
    Nemeti M, Louie E, Papp Z, Johnson JP.
    Hum Genet; 1991 Aug 01; 87(4):511-2. PubMed ID: 1715311
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