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Journal Abstract Search

155 related items for PubMed ID: 3010714

  • 41. Isolation of a polymorphic genomic clone from chromosome 7. Physical and genetic linkage studies to markers around the cystic fibrosis locus.
    Davies KA, Lorand L, Waterfield M, Wainwright B, Farrall M, Williamson R.
    Hum Genet; 1987 Oct; 77(2):122-6. PubMed ID: 2888718
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  • 42. Three additional DNA polymorphisms in the met gene and D7S8 locus: use in prenatal diagnosis of cystic fibrosis.
    Dean M, O'Connell P, Leppert M, Park M, Amos JA, Phillips DG, White R, Vande Woude GF.
    J Pediatr; 1987 Oct; 111(4):490-5. PubMed ID: 2888841
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  • 43. [Indirect cystic fibrosis carrier detection in two Chilean families by analysis of DNA polymorphisms closely linked to the CFTR gene].
    Riveros K N, Ríos H J.
    Rev Med Chil; 2005 Jun; 133(6):648-54. PubMed ID: 16075128
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  • 44. Exclusion of catalytic and regulatory subunits of cAMP-dependent protein kinase as candidate genes for the defect causing cystic fibrosis.
    Scambler P, Oyen O, Wainwright B, Farrall M, Law HY, Estivill X, Sandberg M, Williamson R, Jahnsen T.
    Am J Hum Genet; 1987 Nov; 41(5):925-32. PubMed ID: 3479018
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  • 45. Linkage of DNA probe B79a (D7S13) to cystic fibrosis.
    Wainwright BJ, Tsui LC, Leppert M, Buchwald M, Estivill X, O'Connell P, Lathrop M, Lalouel JM, White R, Williamson R.
    Am J Hum Genet; 1987 Nov; 41(5):944-7. PubMed ID: 2890297
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  • 46. 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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  • 47. A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis.
    Ramsay M, Wainwright BJ, Farrall M, Estivill X, Sutherland H, Ho MF, Davies R, Halford S, Tata F, Wicking C.
    Genomics; 1990 Jan; 6(1):39-47. PubMed ID: 1968045
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  • 48. Highly polymorphic RFLP probes as diagnostic tools.
    Donis-Keller H, Barker DF, Knowlton RG, Schumm JW, Braman JC, Green P.
    Cold Spring Harb Symp Quant Biol; 1986 Jan; 51 Pt 1():317-24. PubMed ID: 2884062
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  • 50. Homogeneity of cystic fibrosis in Italy.
    Vitale E, Devoto M, Mastella G, Romeo G.
    Am J Hum Genet; 1986 Dec; 39(6):832-6. PubMed ID: 3467589
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  • 51. Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis.
    Klinger KW, Winqvist R, Riccio A, Andreasen PA, Sartorio R, Nielsen LS, Stuart N, Stanislovitis P, Watkins P, Douglas R.
    Proc Natl Acad Sci U S A; 1987 Dec; 84(23):8548-52. PubMed ID: 2891140
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  • 52. [Genetic study in 8 families with a child with cystic fibrosis].
    Riedler J, Arrer E, Grabherr B.
    Wien Klin Wochenschr; 1989 Sep 01; 101(16):548-51. PubMed ID: 2572089
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  • 60. Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populations.
    Estivill X, Gasparini P, Novelli G, Casals T, Nunes V, Gallano P, Savoia A, Ruzzo A, Dallapiccola B, Pignatti PF.
    Hum Genet; 1989 Sep 01; 83(2):175-8. PubMed ID: 2777258
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