These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

266 related items for PubMed ID: 6232534

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].
    Lambotte C.
    Rev Med Liege; 1986 Jan 15; 41(2):37-44. PubMed ID: 3006204
    [No Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluid.
    Gueux B, Fiet J, Couillin P, Raux-Demay MC, Mornet E, Galons H, Villette JM, Boue J, Dreux C.
    J Clin Endocrinol Metab; 1988 Mar 15; 66(3):534-7. PubMed ID: 3258316
    [Abstract] [Full Text] [Related]

  • 4. 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 Mar 15; 6(4):295-300. PubMed ID: 7211946
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 73(4):358-64. PubMed ID: 3017844
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. [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 Aug 15; 111(9-10):312-7. PubMed ID: 2633007
    [Abstract] [Full Text] [Related]

  • 12. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients.
    Livieri C, Belvedere M, Martinetti M, Beluffi G, Fiori P, Cogliati CR, Goffredo V, Lorini R, Severi F.
    Prog Clin Biol Res; 1985 Aug 15; 200():243-55. PubMed ID: 3001775
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Particular interest of HLA typing for genetic counselling in families with congenital adrenal hyperplasia (21-OH deficiency).
    Couillin P, Boué J, Bétuel H, Hors J, Gebuhrer L, Boué A.
    Haematologia (Budap); 1987 Aug 15; 20(1):25-30. PubMed ID: 3496258
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: comparison with HLA typing in 17 pregnancies at risk for CAH.
    Forest MG, Bétuel H, Couillin P, Boué A.
    Prenat Diagn; 1981 Jul 15; 1(3):197-207. PubMed ID: 6981108
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype].
    Dzenis IG, Brykova EK, Bakharev VA.
    Akush Ginekol (Mosk); 1990 Jan 15; (1):10-4. PubMed ID: 2353725
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [Prenatal diagnosis of congenital adrenal hyperplasia due to a 21-hydroxylase defect--determination of 17-hydroxyprogesterone in the amniotic fluid].
    Dumić M, Plavsić V, Ille J, Brkljacić L, Drazanćić A, Suchanek E, Kaśtelan A.
    Lijec Vjesn; 1987 Jan 15; 109(2-3):65-7. PubMed ID: 3496509
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.