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

134 related items for PubMed ID: 86832

  • 1. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.
    Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon M, Owens RP, Merkatz IR, Nitowsky BM, Sachs G, Dupont B.
    Lancet; 1979 May 26; 1(8126):1107-8. PubMed ID: 86832
    [Abstract] [Full Text] [Related]

  • 2. HLA typing of amniotic-fluid cells applied to prenatal diagnosis of congenital adrenal hyperplasia.
    Couillin P, Nicolas H, Boué J, Boué A.
    Lancet; 1979 May 19; 1(8125):1076. PubMed ID: 86789
    [No Abstract] [Full Text] [Related]

  • 3. 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 19; 8(2):131-43. PubMed ID: 3258985
    [Abstract] [Full Text] [Related]

  • 4. Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Dupont B, Oberfield SE, Smithwick EM, Lee TD, Levine LS.
    Lancet; 1988 Feb 19; 2(8052-8053):1309-12. PubMed ID: 74726
    [Abstract] [Full Text] [Related]

  • 5. HLA and congenital adrenal hyperplasia linkage confirmed.
    Lancet; 1978 Apr 29; 1(8070):930-2. PubMed ID: 76861
    [No Abstract] [Full Text] [Related]

  • 6. 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 29; 1(1):25-33. PubMed ID: 6955777
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Milunsky A, Tulchinsky D.
    Pediatrics; 1977 May 29; 59(5):768-70. PubMed ID: 558577
    [No Abstract] [Full Text] [Related]

  • 8. 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 May 29; 6(4):295-300. PubMed ID: 7211946
    [Abstract] [Full Text] [Related]

  • 9. Antenatal diagnosis of congenital adrenal hyperplasia.
    Hughes IA, Laurence KM.
    Lancet; 1979 Jul 07; 2(8132):7-9. PubMed ID: 87946
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [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 07; 1(3):183-95. PubMed ID: 6981107
    [Abstract] [Full Text] [Related]

  • 12. 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 07; 11(4):1726-8. PubMed ID: 394430
    [No Abstract] [Full Text] [Related]

  • 13. 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 07; 61(1):89-97. PubMed ID: 3873469
    [Abstract] [Full Text] [Related]

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

  • 15. 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 07; 1(3):197-207. PubMed ID: 6981108
    [Abstract] [Full Text] [Related]

  • 16. 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 Jul 07; 458():148-55. PubMed ID: 3937472
    [No Abstract] [Full Text] [Related]

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

  • 18. [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 Jul 07; 111(9-10):312-7. PubMed ID: 2633007
    [Abstract] [Full Text] [Related]

  • 19. [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]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.