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Journal Abstract Search

116 related items for PubMed ID: 3573974

  • 1. [Prenatal detection of congenital adrenal hyperplasia using HLA typing of fetal cells from the amniotic fluid].
    Brkljacić L, Dumić M, Plavsić V, Drazancić A, Gerencer M, Kastelan A.
    Lijec Vjesn; 1986; 108(11-12):497-500. PubMed ID: 3573974
    [No Abstract] [Full Text] [Related]

  • 2. 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; 6(4):295-300. PubMed ID: 7211946
    [Abstract] [Full Text] [Related]

  • 3. [Methodology for HLA typing of amniotic fluid fetal cells (author's transl)].
    Couillin P, Nicolas H, Grisard MC, Boué J, Boué A.
    Ann Genet; 1980; 23(1):40-5. PubMed ID: 6965839
    [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; 111(9-10):312-7. PubMed ID: 2633007
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of congenital adrenal hyperplasia.
    Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.
    Am J Med Genet; 1979; 4(2):201-4. PubMed ID: 517576
    [Abstract] [Full Text] [Related]

  • 6. 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; 8(2):131-43. PubMed ID: 3258985
    [Abstract] [Full Text] [Related]

  • 7. [Possibilities of prenatal diagnosis of the adrenogenital syndrome using HLA typing of cultivated amnion cells].
    Wurster KG, Clemens GE, Schunter F, Heilbronner H.
    Dtsch Med Wochenschr; 1979 Apr 06; 104(14):526. PubMed ID: 436616
    [No Abstract] [Full Text] [Related]

  • 8. [Pregnanetriol in the amniotic fluid: prenatal diagnosis of adrenogenital syndrome by amniocentesis (author's transl)].
    Holzmann K, Wittenbecher G, Mickan H.
    Geburtshilfe Frauenheilkd; 1974 May 06; 34(5):364-8. PubMed ID: 4849448
    [No Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. [Prenatal diagnosis of congenital hyperplasia of the adrenal cortex].
    Dzenis IG, Brykova EK, Bronshteĭn MI, Bakharev VA, Fanchenko ND.
    Sov Med; 1988 Apr 21; (7):11-4. PubMed ID: 3227442
    [No Abstract] [Full Text] [Related]

  • 11. Technical and theoretical considerations in the HLA typing of amniotic fluid cells for prenatal diagnosis and paternity testing.
    Pollack MS, Heagney SD, Braun D, O'Neill GJ.
    Prenat Diagn; 1981 Jul 21; 1(3):183-95. PubMed ID: 6981107
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of congenital adrenal hyperplasia.
    Warsof SL, Larsen JW, Kent SG, Rosenbaum KN, August GP, Migeon CJ, Schulman JD.
    Obstet Gynecol; 1980 Jun 21; 55(6):751-4. PubMed ID: 7383464
    [Abstract] [Full Text] [Related]

  • 13. 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 21; 66(3):534-7. PubMed ID: 3258316
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of congenital lipoid adrenal hyperplasia.
    Izumi H, Saito N, Ichiki S, Makino Y, Yukitake K, Kaneoka T.
    Obstet Gynecol; 1993 May 21; 81(5 ( Pt 2)):839-41. PubMed ID: 8469492
    [Abstract] [Full Text] [Related]

  • 15. [Antenatal detection of congenital adrenal hyperplasia. Deficiency of 21-hydroxylase].
    Floret D, Plauchu H, Berlin F, Betuel H, Forest M.
    Nouv Presse Med; 1980 Jun 28; 9(28):1960-1. PubMed ID: 6968432
    [No Abstract] [Full Text] [Related]

  • 16. [Utilization of chromosome markers and HLA antigens for prenatal identification of the male parent in artificial insemination for genetic reasons (author's transl)].
    Boué J, Couillin P, Yvert F.
    Sem Hop; 1980 Jun 28; 57(3-4):117-20. PubMed ID: 6261349
    [Abstract] [Full Text] [Related]

  • 17. [Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies].
    Nivelon JL, Chouchane M, Forest MG, Morel Y, Huet F, Nivelon-Chevallier A, François C.
    Ann Pediatr (Paris); 1993 Sep 28; 40(7):421-5. PubMed ID: 7902059
    [Abstract] [Full Text] [Related]

  • 18. [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 Sep 28; 109(2-3):65-7. PubMed ID: 3496509
    [No Abstract] [Full Text] [Related]

  • 19. 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 Sep 28; 458():148-55. PubMed ID: 3937472
    [No Abstract] [Full Text] [Related]

  • 20. Tissue typing amniotic fluid cells: potential use for detection of contaminating maternal cells.
    Niazi M, Coleman DV, Mowbray JF, Blunt S.
    J Med Genet; 1979 Feb 28; 16(1):21-3. PubMed ID: 469881
    [Abstract] [Full Text] [Related]

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