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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 86789)

  • 21. Prenatal diagnosis of congenital adrenal hyperplasia.
    New MI
    Prog Clin Biol Res; 1976; 10():205-19. PubMed ID: 799794
    [No Abstract]   [Full Text] [Related]  

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

  • 23. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 25. Congenital and acquired disorders of the adrenal cortex.
    Hughes IA
    Clin Endocrinol Metab; 1982 Mar; 11(1):89-125. PubMed ID: 7047023
    [No Abstract]   [Full Text] [Related]  

  • 26. Possible genetic linkage disequilibrium between HLA and the 21-hydroxylase deficiency gene (congenital adrenal hyperplasia).
    Pollack MS; Levine L; Zachmann M; Prader A; New M; Oberfield S; Dupont B
    Transplant Proc; 1979 Jun; 11(2):1315-6. PubMed ID: 314176
    [No Abstract]   [Full Text] [Related]  

  • 27. 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; 66(3):534-7. PubMed ID: 3258316
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Amniotic fluid levels of 17 alpha-hydroxyprogesterone during human pregnancy: pre-natal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Wurster KG; Ranke MB; Heilbronner H; Gupta D
    Endokrinologie; 1982 Oct; 80(2):142-50. PubMed ID: 6984387
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of congenital adrenal hyperplasia.
    Levine LS; New MI; Pollack M; Dupont B
    Lancet; 1979 Sep; 2(8143):637. PubMed ID: 90299
    [No Abstract]   [Full Text] [Related]  

  • 30. [The significance of genetic examination in the diagnosis of inborn adrenal hyperplasia].
    Srsen S
    Cesk Pediatr; 1977 Sep; 32(9):541-2. PubMed ID: 597946
    [No Abstract]   [Full Text] [Related]  

  • 31. Is prenatal HLA typing of uncultured amniocytes before the collection of related allogenic cord blood helpful?
    Zieger W; Meckies J; Eichler H; Melchert F; Bugert P
    Arch Gynecol Obstet; 2003 Feb; 267(4):230-2. PubMed ID: 12592425
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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; 61(1):89-97. PubMed ID: 3873469
    [TBL] [Abstract][Full Text] [Related]  

  • 33. HLA and congenital adrenal hyperplasia.
    Lancet; 1978 Nov; 2(8098):1046-7. PubMed ID: 82057
    [No Abstract]   [Full Text] [Related]  

  • 34. [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; 1981 Jan 18-25; 57(3-4):117-20. PubMed ID: 6261349
    [TBL] [Abstract][Full Text] [Related]  

  • 35. HLA typing of amniotic fluid cells.
    Adinolfi M
    Prenat Diagn; 1982 Apr; 2(2):147. PubMed ID: 7145842
    [No Abstract]   [Full Text] [Related]  

  • 36. Antenatal detection of congenital adrenal hyperplasia.
    Sibert JR
    Lancet; 1979 Jul; 2(8132):37. PubMed ID: 87907
    [No Abstract]   [Full Text] [Related]  

  • 37. Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Dupont B; Oberfield SE; Smithwick EM; Lee TD; Levine LS
    Lancet; 1977 Dec 24-31; 2(8052-8053):1309-12. PubMed ID: 74726
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Serum HLA typing.
    Tait BD; Finlay RI; Simons MJ
    Tissue Antigens; 1981 Feb; 17(2):129-35. PubMed ID: 7233413
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Lymphocyte suspensions greater than 2000/l per microliter sensitize HLA typing].
    Májský A
    Vnitr Lek; 1987 May; 33(5):468-71. PubMed ID: 3604068
    [No Abstract]   [Full Text] [Related]  

  • 40. Prognostic value of antibody-dependent assays for presensitization in bone marrow transplant recipients.
    Parkman R; Rappeport J; Camitta B; Levey R; Rosen FS
    Transplant Proc; 1978 Mar; 10(1):71-3. PubMed ID: 345568
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.