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Journal Abstract Search

199 related items for PubMed ID: 7896301

  • 1. 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; 45(1):55-7. PubMed ID: 7896301
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  • 4. 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
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  • 5. The incidence of delta F508 CF mutation, and associated haplotypes, in a sample of English CF families.
    Watson EK, Mayall ES, Simova L, Thompson EM, Warner JO, Williamson R, Williams C.
    Hum Genet; 1990 Sep; 85(4):435-6. PubMed ID: 2210766
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  • 8. Frequency of the delta F508 mutation on cystic fibrosis chromosomes in Denmark.
    Schwartz M, Johansen HK, Koch C, Brandt NJ.
    Hum Genet; 1990 Sep; 85(4):427-8. PubMed ID: 2210762
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  • 10. 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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  • 11. 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
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  • 13. 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; 48(2):223-6. PubMed ID: 1990833
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  • 15. 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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