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Journal Abstract Search

216 related items for PubMed ID: 2210767

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  • 2. 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
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  • 3. 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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  • 4. 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 01; 87(1):61-4. PubMed ID: 2037283
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  • 7. 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 01; 85(4):419-20. PubMed ID: 2210756
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  • 11. Frequency of the delta F508 mutation on cystic fibrosis chromosomes in Denmark.
    Schwartz M, Johansen HK, Koch C, Brandt NJ.
    Hum Genet; 1990 Sep 01; 85(4):427-8. PubMed ID: 2210762
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  • 12. Cystic fibrosis haplotype association and the delta F508 mutation in adult British CF patients.
    Santis G, Osborne L, Knight R, Ramsay M, Williamson R, Hodson M.
    Hum Genet; 1990 Sep 01; 85(4):424-5. PubMed ID: 2210760
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  • 13. 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 01; 85(4):402-3. PubMed ID: 2210747
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  • 15. A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation origin.
    Chehab FF, Johnson J, Louie E, Goossens M, Kawasaki E, Erlich H.
    Am J Hum Genet; 1991 Feb 01; 48(2):223-6. PubMed ID: 1990833
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