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Journal Abstract Search

102 related items for PubMed ID: 2215505

  • 1. [Direct genetic diagnosis in cystic fibrosis].
    Reiss J, Schlösser M, Wagner M, Lenz U, Krawczak M, Ammann G, Klösser S, Böwing B.
    Monatsschr Kinderheilkd; 1990 Aug; 138(8):434-7. PubMed ID: 2215505
    [Abstract] [Full Text] [Related]

  • 2. [Detection of carriers and prenatal diagnosis of cystic fibrosis in Spanish families using DNA markers].
    Baiget M, Casals T, Nunes V, Estivill X.
    Med Clin (Barc); 1989 Mar 18; 92(10):361-3. PubMed ID: 2716384
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  • 3. [DNA diagnosis of monogene hereditary diseases exemplified by phenylketonuria and mucoviscidosis].
    Trefz FK, Lichter-Konecki U, Krawczak M, Schmidtke J, Dueck M, Nützenadel W, Konecki DS.
    Monatsschr Kinderheilkd; 1989 Apr 18; 137(4):201-7. PubMed ID: 2659975
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  • 4. Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis.
    Dry PJ, Wake S, Robertson CF, Colley P, Sheffield LJ.
    Med J Aust; 1989 Aug 07; 151(3):131, 133-6. PubMed ID: 2569157
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  • 5. Genotyping of cystic fibrosis families with linked DNA probes.
    Curtis A, Strain L, Brock DJ.
    Clin Genet; 1988 Jan 07; 33(1):53-6. PubMed ID: 2893675
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  • 6. [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
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  • 13. [Carrier detection and prenatal diagnosis in phenylketonuria, cystic fibrosis and adrenal hyperplasia use of molecular biology techniques].
    Orgad S, Yaar L, Barkai G, Avigad S, Lieberman A, Goldmann B, Gazit E.
    Harefuah; 1989 Mar 15; 116(6):297-300. PubMed ID: 2731793
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  • 16. Reproductive decision making of aunts and uncles of a child with cystic fibrosis: genetic risk perception and attitudes toward carrier identification and prenatal diagnosis.
    Denayer L, Evers-Kiebooms G, De Boeck K, Van den Berghe H.
    Am J Med Genet; 1992 Sep 01; 44(1):104-11. PubMed ID: 1519639
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  • 17. [Carrier detection in cystic fibrosis. Various illustrative examples].
    Kroes HY, Scheffer H, ten Kate LP.
    Tijdschr Kindergeneeskd; 1992 Dec 01; 60(6):226-30. PubMed ID: 1488735
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  • 18. [Molecular diagnosis of cystic fibrosis].
    Malik NJ, Hergersberg M.
    Ther Umsch; 1995 Dec 01; 52(12):801-4. PubMed ID: 8539650
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  • 19. [Direct diagnosis of predominant mutation delta F508 associated with the mucoviscidosis gene].
    Férec C, Guillermit H, Verlingue C, Parent P, Puissant H, Jehanne M, Saleun JP.
    Arch Fr Pediatr; 1990 Dec 01; 47(7):507-10. PubMed ID: 2256790
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  • 20. [Determination of haplotypes of DNA markers linked to the mucoviscidosis locus: detection of heterozygotes].
    Vasseur F, Fontaine F, Savary JB, Deminatti MM.
    Ann Genet; 1988 Dec 01; 31(2):97-101. PubMed ID: 2840848
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