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Journal Abstract Search

158 related items for PubMed ID: 1870597

  • 41. Prenatal diagnosis of cystic fibrosis: a case of twin pregnancy diagnosis and a review of 5 years' experience.
    Castaldo G, Martinelli P, Massa C, Fuccio A, Grosso M, Rippa E, Paladini D, Salvatore F.
    Clin Chim Acta; 2000 Aug; 298(1-2):121-33. PubMed ID: 10876009
    [Abstract] [Full Text] [Related]

  • 42. Molecular screening of cystic fibrosis patients.
    Fellowes AP, Murphy JM, Wesley AW, Dawson KP, George PM.
    N Z Med J; 1991 Oct 09; 104(921):415-6. PubMed ID: 1923090
    [Abstract] [Full Text] [Related]

  • 43. Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family.
    Lucotte G, Berriche S, David F, Mariotti M, Turpin JC.
    Genet Couns; 1994 Oct 09; 5(2):171-4. PubMed ID: 7917127
    [Abstract] [Full Text] [Related]

  • 44. [Diagnosis of cystic fibrosis based on restriction fragment length polymorphism of DNA].
    Burg K, Endreffy E, Berekk I, Gyurkovits K, László A, Petri I, Kaiser G, Raskó I.
    Orv Hetil; 1987 Dec 06; 128(49):2571-2, 2575. PubMed ID: 3325874
    [No Abstract] [Full Text] [Related]

  • 45. Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at 1-in-4 risk.
    Feldman GL, Lewiston N, Fernbach SD, O'Brien WE, Williamson R, Wainwright BJ, Beaudet AL.
    Am J Med Genet; 1989 Jun 06; 33(2):238-41. PubMed ID: 2569827
    [Abstract] [Full Text] [Related]

  • 46. Genetic counseling and prenatal diagnosis of cystic fibrosis.
    Fisher NL.
    Am J Obstet Gynecol; 1979 Nov 01; 135(5):699. PubMed ID: 507123
    [No Abstract] [Full Text] [Related]

  • 47. Changing patterns of genetic counseling in a cystic fibrosis center.
    Gluckson MM, Denning CR.
    Prog Clin Biol Res; 1979 Nov 01; 34():119-32. PubMed ID: 531050
    [No Abstract] [Full Text] [Related]

  • 48. Circulating trophoblastic cells provide genetic diagnosis in 63 fetuses at risk for cystic fibrosis or spinal muscular atrophy.
    Mouawia H, Saker A, Jais JP, Benachi A, Bussières L, Lacour B, Bonnefont JP, Frydman R, Simpson JL, Paterlini-Brechot P.
    Reprod Biomed Online; 2012 Nov 01; 25(5):508-20. PubMed ID: 23000084
    [Abstract] [Full Text] [Related]

  • 49. Prenatal genetic carrier testing using triple disease screening.
    Eng CM, Schechter C, Robinowitz J, Fulop G, Burgert T, Levy B, Zinberg R, Desnick RJ.
    JAMA; 1997 Oct 15; 278(15):1268-72. PubMed ID: 9333269
    [Abstract] [Full Text] [Related]

  • 50. [Mucoviscidosis: current diagnostic possibilities. Applications in perinatology].
    Ferec C, Chabaud JJ, Parent P, Dewitte JD, Verlingue C, Clavier J, Saleun JP.
    Rev Mal Respir; 1989 Oct 15; 6(1):45-52. PubMed ID: 2564690
    [Abstract] [Full Text] [Related]

  • 51. [Cystic fibrosis. Prenatal diagnosis].
    Herrera M, Ruiz M, Kunkar L.
    Rev Chil Obstet Ginecol; 1991 Oct 15; 56(2):117-21; discussion 121-3. PubMed ID: 1844608
    [Abstract] [Full Text] [Related]

  • 52. [Prenatal diagnosis of cystic fibrosis using DNA analysis].
    Halley DJ, Morreau J, Neijens HJ, van Swaay E, Sandkuyl LA, Oostra BA.
    Ned Tijdschr Geneeskd; 1986 Dec 13; 130(50):2270-2. PubMed ID: 3027590
    [No Abstract] [Full Text] [Related]

  • 53. Population-based carrier screening for cystic fibrosis in Victoria: the first three years experience.
    Massie J, Petrou V, Forbes R, Curnow L, Ioannou L, Dusart D, Bankier A, Delatycki M.
    Aust N Z J Obstet Gynaecol; 2009 Oct 13; 49(5):484-9. PubMed ID: 19780730
    [Abstract] [Full Text] [Related]

  • 54. Compound heterozygosity for delta F508 and F508C: a cautionary note on the molecular diagnosis of cystic fibrosis.
    Dufourcq R, Vuillaumier S, Pascaud O, Guidal C, Oury JF, Elion J, Denamur E.
    Prenat Diagn; 1994 Dec 13; 14(12):1176-7. PubMed ID: 7899288
    [No Abstract] [Full Text] [Related]

  • 55. Molecular screening of partners of cystic fibrosis heterozygotes.
    Shrimpton AE, Brock DJ.
    Genet Couns; 1992 Dec 13; 3(1):13-8. PubMed ID: 1375470
    [Abstract] [Full Text] [Related]

  • 56. Cystic fibrosis--2: genetic and social aspects.
    Russell G.
    Nurs Times; 1978 Mar 30; 74(13):538-41. PubMed ID: 628612
    [No Abstract] [Full Text] [Related]

  • 57. Parental understanding of newborn screening for cystic fibrosis after a negative sweat-test.
    Lang CW, McColley SA, Lester LA, Ross LF.
    Pediatrics; 2011 Feb 30; 127(2):276-83. PubMed ID: 21220393
    [Abstract] [Full Text] [Related]

  • 58. Usefulness of linked DNA probes for prenatal diagnosis of cystic fibrosis: report of a case in a 1:4 risk pregnancy.
    Fontaine F, Vasseur F, Savary JB, Menais M, Roussel M, Deminatti MM.
    Ann Genet; 1988 Feb 30; 31(2):102-4. PubMed ID: 2840846
    [Abstract] [Full Text] [Related]

  • 59. Prenatal diagnosis of cystic fibrosis using closely linked DNA probes.
    Lissens W, Vercammen M, Foulon W, De Catte L, Dab I, Malfroot A, Bonduelle M, Liebaers I.
    J Inherit Metab Dis; 1989 Feb 30; 12 Suppl 2():308-10. PubMed ID: 2574253
    [No Abstract] [Full Text] [Related]

  • 60. [Progress in the analysis of cystic fibrosis: prenatal diagnosis and carrier detection].
    Estivill X.
    Med Clin (Barc); 1989 Mar 18; 92(10):375-7. PubMed ID: 2565992
    [No Abstract] [Full Text] [Related]

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