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Journal Abstract Search

91 related items for PubMed ID: 394430

  • 1. HLA typing of amniotic cells: the prenatal diagnosis of congenital adrenal hyperplasia (21-OH-deficiency type).
    Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon MA, Owens RP, Merkatz IR, Nitowsky HM, Sachs G, Dupont B.
    Transplant Proc; 1979 Dec; 11(4):1726-8. PubMed ID: 394430
    [No Abstract] [Full Text] [Related]

  • 2. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Couillin P.
    Presse Med; 1984 Apr 21; 13(17):1087-90. PubMed ID: 6232534
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  • 3. The use of gamma interferon to increase HLA antigen expression on cultured amniotic cells used for the prenatal diagnosis of 21-hydroxylase deficiency.
    Maurer DH, Pollack MS.
    Ann N Y Acad Sci; 1985 Apr 21; 458():148-55. PubMed ID: 3937472
    [No Abstract] [Full Text] [Related]

  • 4. [Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase enzyme deficiency].
    Dumić M, Ille J, Brkljacić L, Plavsić V, Drazancić A, Banicević M, Radmanović S, Filipović B, Suchanek E, Kastelan A.
    Lijec Vjesn; 1989 Apr 21; 111(9-10):312-7. PubMed ID: 2633007
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  • 6. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI.
    J Clin Endocrinol Metab; 1985 Jul 21; 61(1):89-97. PubMed ID: 3873469
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  • 7. HLA-A,B,C,DR typing and 17-OHP determination for second trimester prenatal diagnosis of 21-hydroxylase deficient CAH.
    Grosse-Wilde H, Valentine-Thon E, Vögeler U, Passarge E, Lorenzen F, Sippell WG, Bidlingmaier F, Knorr D.
    Prenat Diagn; 1988 Feb 21; 8(2):131-43. PubMed ID: 3258985
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  • 8. [Genetic of the 21 hydroxylase deficiency].
    Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.
    Ann Endocrinol (Paris); 1982 Feb 21; 43(1):3-14. PubMed ID: 6982657
    [Abstract] [Full Text] [Related]

  • 9. Amniotic 17-alpha hydroxyprogesterone and HLA typing for the prenatal diagnosis of 21-alpha hydroxylase deficiency--congenital adrenal hyperplasia.
    Rosenmann A, Schumert Z, Theodor R, Cohen T, Brautbar C.
    Am J Med Genet; 1980 Feb 21; 6(4):295-300. PubMed ID: 7211946
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  • 15. Prenatal diagnosis of 21-hydroxylase deficiency.
    Prenat Diagn; 1988 Mar 21; 8(3):245-6. PubMed ID: 3259695
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  • 16. Prenatal diagnosis of congenital adrenal hyperplasia (21-OH deficiency type) by HLA typing.
    Couillin P, Boue J, Nicolas H, Cheruy C, Boue A.
    Prenat Diagn; 1981 Jan 21; 1(1):25-33. PubMed ID: 6955777
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  • 17. First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
    Mornet E, Boue J, Raux-Demay M, Couillin P, Oury JF, Dumez Y, Dausset J, Cohen D, Boué A.
    Hum Genet; 1986 Aug 21; 73(4):358-64. PubMed ID: 3017844
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  • 19. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI.
    Ann N Y Acad Sci; 1985 Aug 21; 458():111-29. PubMed ID: 3879117
    [No Abstract] [Full Text] [Related]

  • 20. Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes.
    Raux-Demay M, Mornet E, Boue J, Couillin P, Oury JF, Ravise N, Deluchat C, Boue A.
    Prenat Diagn; 1989 Jul 21; 9(7):457-66. PubMed ID: 2788885
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