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Journal Abstract Search

106 related items for PubMed ID: 2811875

  • 1. [An at-risk pregnancy of a carrier of cystic fibrosis (mucoviscidosis) with a new partner].
    Reiss J, Krawczak M, Gal A, Zerres K, Kaiser R, Weber J.
    Monatsschr Kinderheilkd; 1989 Aug; 137(8):451-3. PubMed ID: 2811875
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  • 2. [Genetic counseling in prenatal diagnosis of cystic fibrosis].
    Wolff G, Mayerová A.
    Monatsschr Kinderheilkd; 1991 May; 139(5):275-81. PubMed ID: 1870597
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  • 3. [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 May; 31(2):97-101. PubMed ID: 2840848
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  • 4. [Analysis of 112 haplotypes carrying the cystic fibrosis gene. Applications in genetic counseling].
    Parent P, Ferec C, Morin JF, Chabaud JJ.
    J Genet Hum; 1989 Jun; 37(2):133-40. PubMed ID: 2746172
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  • 5. [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
    [Abstract] [Full Text] [Related]

  • 6. Identification of carriers by screening for delta F508 deletion in a multi-generation cystic fibrosis family.
    Claustres M, Desgeorges M, Kjellberg P, Demaille J.
    Genet Couns; 1990 Mar 18; 1(3-4):211-7. PubMed ID: 1982988
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  • 7. Cystic fibrosis. Part II. New developments in cystic fibrosis--implications for carrier detection and genetic counselling.
    Denter M, Ramsay M, Jenkins T.
    S Afr Med J; 1992 Jul 18; 82(1):11-3. PubMed ID: 1641710
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. [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 01; 138(8):434-7. PubMed ID: 2215505
    [Abstract] [Full Text] [Related]

  • 10. [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 Aug 01; 47(7):507-10. PubMed ID: 2256790
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  • 15. Testing and reporting ACMG cystic fibrosis mutation panel results.
    Lebo RV, Grody WW.
    Genet Test; 2007 Aug 01; 11(1):11-31. PubMed ID: 17394390
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  • 16. Carrier screening for cystic fibrosis.
    Dungan JS.
    Obstet Gynecol Clin North Am; 2010 Mar 01; 37(1):47-59, Table of Contents. PubMed ID: 20494257
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  • 20. [Early detection, heterozygote diagnosis and prenatal diagnosis in cystic fibrosis (mucoviscidosis)].
    Hein J.
    Kinderarztl Prax; 1982 Apr 01; 50(4):186-95. PubMed ID: 7109464
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