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Journal Abstract Search

134 related items for PubMed ID: 2013712

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  • 3. 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; 62(5):995-1002. PubMed ID: 3007562
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  • 4. Restriction fragment length polymorphism study of families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Taiwan.
    Lee JS, Tsai HM, Shieh RP, Chen SH, Tsai WY, Chung BC.
    J Formos Med Assoc; 1990 Jul; 89(7):534-40. PubMed ID: 1979594
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  • 5. Prenatal diagnosis of 21-hydroxylase deficiency by RFLP analysis of the 21-hydroxylase, complement C4, and HLA class II genes.
    Keller E, Andreas A, Scholz S, Dörr HC, Knorr D, Albert ED.
    Prenat Diagn; 1991 Nov; 11(11):827-40. PubMed ID: 1684434
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  • 6. 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
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  • 7. TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiency.
    Olerup O, Luthman H, Ritzén EM, Haglund-Stengler B.
    Hum Genet; 1990 Oct; 85(5):467-72. PubMed ID: 1977680
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  • 8. A case of first trimester prenatal diagnosis of 21-hydroxylase deficiency with human complement C4 cDNA probe.
    Nakura J, Miki T, Nishikawa K, Takemoto Y, Kamino K, Takai S, Hayashi K, Ogihara T.
    Endocrinol Jpn; 1990 Oct; 37(5):615-8. PubMed ID: 1982260
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  • 9. 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
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  • 11. Highly polymorphic XbaI RFLPs of the human 21-hydroxylase genes among Chinese.
    Chen L, Pan X, Shen Y, Chen Z, Zhang Y, Chen R.
    J Med Genet; 1992 Apr; 29(4):231-2. PubMed ID: 1349921
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  • 12. First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
    Mornet E, Boue J, Raux-Demay M, Couillin P, Oury JF, Dumez Y, Dausset J, Cohen D, Boué A.
    Hum Genet; 1986 Aug; 73(4):358-64. PubMed ID: 3017844
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  • 13. 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 Aug; 30 Suppl():111-6. PubMed ID: 2906201
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  • 14. [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
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  • 15. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.
    White PC, New MI, Dupont B.
    Proc Natl Acad Sci U S A; 1984 Dec 20; 81(23):7505-9. PubMed ID: 6334310
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  • 17. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency).
    Speiser PW, Laforgia N, Kato K, Pareira J, Khan R, Yang SY, Whorwood C, White PC, Elias S, Schriock E.
    J Clin Endocrinol Metab; 1990 Apr 20; 70(4):838-48. PubMed ID: 1969421
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  • 20. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A paradigm for prenatal diagnosis and treatment.
    Nimkarn S, New MI.
    Ann N Y Acad Sci; 2010 Mar 20; 1192():5-11. PubMed ID: 20392211
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