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

176 related items for PubMed ID: 1801590

  • 1. Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Morel Y, Miller WL.
    Adv Hum Genet; 1991; 20():1-68. PubMed ID: 1801590
    [No 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. Congenital adrenal hyperplasia.
    Wedell A.
    Clin Biochem; 2011 May 15; 44(7):505-506. PubMed ID: 22036349
    [No 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 May 15; 6(4):295-300. PubMed ID: 7211946
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.
    O'Neill GJ, Dupont B, Pollack MS, Levine LS, New MI.
    Clin Immunol Immunopathol; 1982 May 21; 23(2):312-22. PubMed ID: 6980755
    [No Abstract] [Full Text] [Related]

  • 7. Adrenal 21-hydroxylase cytochrome P-450 genes within the MHC class III region.
    White PC, New MI, Dupont B.
    Immunol Rev; 1985 Oct 21; 87():123-50. PubMed ID: 3902620
    [Abstract] [Full Text] [Related]

  • 8. 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 Oct 21; 200():243-55. PubMed ID: 3001775
    [No Abstract] [Full Text] [Related]

  • 9. Molecular genetics and the characterization of steroid 21-hydroxylase deficiency.
    New MI.
    Endocr Res; 1986 Oct 21; 12(4):505-22. PubMed ID: 3030723
    [Abstract] [Full Text] [Related]

  • 10. Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.
    Donohoue PA, van Dop C, McLean RH, White PC, Jospe N, Migeon CJ.
    J Clin Endocrinol Metab; 1986 May 21; 62(5):995-1002. PubMed ID: 3007562
    [Abstract] [Full Text] [Related]

  • 11. Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.
    Rumsby G, Fielder AH, Hague WM, Honour JW.
    J Med Genet; 1988 Sep 21; 25(9):596-9. PubMed ID: 3263505
    [Abstract] [Full Text] [Related]

  • 12. Mutations in steroid 21-hydroxylase (CYP21).
    White PC, Tusie-Luna MT, New MI, Speiser PW.
    Hum Mutat; 1994 Sep 21; 3(4):373-8. PubMed ID: 8081391
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of congenital adrenal hyperplasia.
    Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.
    Am J Med Genet; 1979 Jul 21; 4(2):201-4. PubMed ID: 517576
    [Abstract] [Full Text] [Related]

  • 15. Prenatal dexamethasone treatment in pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency: effect on midgestational amniotic fluid steroid levels.
    Dörr HG, Sippell WG.
    J Clin Endocrinol Metab; 1993 Jan 21; 76(1):117-20. PubMed ID: 8421074
    [Abstract] [Full Text] [Related]

  • 16. Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms.
    Balsamo A, Revelli A, Borelli I, Amoroso A, Cenderelli G, De Sanso G, Mazzola G, Curtoni ES, Zoppetti G, Massobrio M.
    Gynecol Endocrinol; 1992 Jun 21; 6(2):91-8. PubMed ID: 1354409
    [Abstract] [Full Text] [Related]

  • 17. Frequent deletion and duplication of the steroid 21-hydroxylase genes.
    Werkmeister JW, New MI, Dupont B, White PC.
    Am J Hum Genet; 1986 Oct 21; 39(4):461-9. PubMed ID: 3490178
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. HLA haplotypes and hormonal studies in 25 Italian families of patients with classical and non-classical 21-OH deficiency.
    Einaudi S, Borelli I, Lala R, Praticŏ L, Curtoni ES, De Sanctis C.
    J Pediatr Endocrinol; 1994 Oct 21; 7(4):349-55. PubMed ID: 7735374
    [Abstract] [Full Text] [Related]

  • 20. Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia.
    Rumsby G, Carroll MC, Porter RR, Grant DB, Hjelm M.
    J Med Genet; 1986 Jun 21; 23(3):204-9. PubMed ID: 3487654
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.