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Journal Abstract Search

232 related items for PubMed ID: 1349559

  • 1. Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia using the polymerase chain reaction.
    Owerbach D, Draznin MB, Carpenter RJ, Greenberg F.
    Hum Genet; 1992 Apr; 89(1):109-10. PubMed ID: 1349559
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of congenital adrenal hyperplasia by direct detection of mutations in the steroid 21-hydroxylase gene.
    Rumsby G, Honour JW, Rodeck C.
    Clin Endocrinol (Oxf); 1993 Apr; 38(4):421-5. PubMed ID: 8319374
    [Abstract] [Full Text] [Related]

  • 3. [21 hydroxylase deficiency: new strategies emerging from molecular studies].
    Morel Y, Tardy V, Costa JM, Forest MG, David M.
    Ann Endocrinol (Paris); 2003 Dec; 64(6):456-70. PubMed ID: 15067252
    [No Abstract] [Full Text] [Related]

  • 4. [CYP21 gene point mutations study in 21-hydroxylase deficiency patients].
    Liao XY, Zhang YF, Gu XF.
    Zhonghua Er Ke Za Zhi; 2003 Sep; 41(9):670-4. PubMed ID: 14733808
    [Abstract] [Full Text] [Related]

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  • 6. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency with DNA analysis.
    Adachi R.
    Nihon Sanka Fujinka Gakkai Zasshi; 1991 Feb; 43(2):227-33. PubMed ID: 2013712
    [Abstract] [Full Text] [Related]

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  • 8. [Abnormal production of adrenal gland hormones--special reference to congenital adrenal hyperplasia].
    Igarashi Y.
    Nihon Naibunpi Gakkai Zasshi; 1991 Jun 20; 67 Suppl 3():740-5. PubMed ID: 1915976
    [No Abstract] [Full Text] [Related]

  • 9. Molecular analysis of the CYP21 gene and prenatal diagnosis in families with 21-hydroxylase deficiency in northeastern Iran.
    Vakili R, Baradaran-Heravi A, Barid-Fatehi B, Gholamin M, Ghaemi N, Abbaszadegan MR.
    Horm Res; 2005 Jun 20; 63(3):119-24. PubMed ID: 15775714
    [Abstract] [Full Text] [Related]

  • 10. RFLPs of 21-hydroxylase and C4 genes: application to pedigree analysis on 21-hydroxylase deficiency.
    Matsumoto T, Kondoh T, Baba T, Yoshimoto M, Niikawa N, Tsuji Y.
    Acta Paediatr Jpn; 1988 Jun 20; 30 Suppl():111-6. PubMed ID: 2906201
    [No Abstract] [Full Text] [Related]

  • 11. Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization.
    Speiser PW, White PC, Dupont J, Zhu D, Mercado A, New MI.
    Recent Prog Horm Res; 1994 Jun 20; 49():367-71. PubMed ID: 8146433
    [Abstract] [Full Text] [Related]

  • 12. Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia.
    Lee HH, Chao HT, Ng HT, Choo KB.
    J Med Genet; 1996 May 20; 33(5):371-5. PubMed ID: 8733045
    [Abstract] [Full Text] [Related]

  • 13. The implication of de novo 21-hydroxylase mutation in clinical and prenatal molecular diagnoses.
    Mao R, McDonald J, Cantwell M, Tang W, Ward K.
    Genet Test; 2005 May 20; 9(2):121-5. PubMed ID: 15943551
    [Abstract] [Full Text] [Related]

  • 14. Fluorescent PCR and automated fragment analysis in preimplantation genetic diagnosis for 21-hydroxylase deficiency in congenital adrenal hyperplasia.
    Van de Velde H, Sermon K, De Vos A, Lissens W, Joris H, Vandervorst M, Van Steirteghem A, Liebaers I.
    Mol Hum Reprod; 1999 Jul 20; 5(7):691-6. PubMed ID: 10381826
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification.
    Theodoropoulou M, Barta C, Szoke M, Guttman A, Staub M, Niederland T, Sólyom J, Fekete G, Sasvari-Szekely M.
    Fetal Diagn Ther; 2001 Jul 20; 16(4):237-40. PubMed ID: 11399887
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot.
    Speiser PW, White PC, Dupont J, Zhu D, Mercado AB, New MI.
    Hum Genet; 1994 Apr 20; 93(4):424-8. PubMed ID: 8168813
    [Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis and treatment of congenital adrenal hyperplasia.
    Nimkarn S, New MI.
    Horm Res; 2007 Apr 20; 67(2):53-60. PubMed ID: 17047340
    [Abstract] [Full Text] [Related]

  • 18. Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese.
    Lee HH, Kuo JM, Chao HT, Lee YJ, Chang JG, Tsai CH, Chung BC.
    J Clin Endocrinol Metab; 2000 Feb 20; 85(2):597-600. PubMed ID: 10690861
    [Abstract] [Full Text] [Related]

  • 19. Altered CYP21 genes in HLA-haplotypes associated with congenital adrenal hyperplasia (CAH): a family study.
    Manfras BJ, Swinyard M, Rudert WA, Ball EJ, Lee PA, Kühnl P, Trucco M, Böhm BO.
    Hum Genet; 1993 Aug 20; 92(1):33-9. PubMed ID: 8365724
    [Abstract] [Full Text] [Related]

  • 20. Sequential use of hydrocortisone and dexamethasone in prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Uçar A, Saka N, Baş F, Poyrazoğlu S, Bundak R, Darendeliler F.
    Horm Res Paediatr; 2013 Aug 20; 79(5):323-4. PubMed ID: 23711741
    [No Abstract] [Full Text] [Related]

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