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Journal Abstract Search

75 related items for PubMed ID: 3492354

  • 1. [Molecular biology of the adrenogenital syndrome. New possibilities of heterozygote screening].
    Böhm BO, Rosak C, Böhm TL, White PC, Schöffling K.
    Dtsch Med Wochenschr; 1987 Jan 16; 112(3):87-9. PubMed ID: 3492354
    [Abstract] [Full Text] [Related]

  • 2. [Genetic of the 21 hydroxylase deficiency].
    Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.
    Ann Endocrinol (Paris); 1982 Jan 16; 43(1):3-14. PubMed ID: 6982657
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  • 3. [Diagnosis of heterozygote carrier of mutant gene of 21-hydroxylase].
    Dzenis IG, Iudina TN, Brykova EK, Bakharev VA, Fanchenko ND.
    Akush Ginekol (Mosk); 1995 Jan 16; (1):21-3. PubMed ID: 7762743
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  • 4. [Adrenogenital syndrome with 21-hydroxylase deficiency].
    Dörr HG, Sippell WG.
    Monatsschr Kinderheilkd; 1993 Jul 16; 141(7):609-21. PubMed ID: 8413342
    [No Abstract] [Full Text] [Related]

  • 5. Glucocorticoid withdrawal - heterozygous carriers of congenital adrenal hyperplasia at risk?
    Brackmann F, Dörr HG, Bartram CR, Hinderhofer K, Holter W, Langer T.
    Klin Padiatr; 2012 Oct 16; 224(6):392-3. PubMed ID: 22915453
    [No Abstract] [Full Text] [Related]

  • 6. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
    Colle M, Battin J.
    Arch Fr Pediatr; 1984 Oct 16; 41(7):483-5. PubMed ID: 6333857
    [Abstract] [Full Text] [Related]

  • 7. [Congenital adrenal hyperplasia].
    Bouvattier C, Chatelain P.
    Rev Prat; 2008 May 15; 58(9):990-4. PubMed ID: 18672665
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  • 9. [Detection of heterozygous carriers of 21-hydroxylase deficiency-HLA typing and endocrinological study (author's transl)].
    Saito N, Kuribayashi T, Shimozawa K, Nakagawa S, Tomita M.
    Horumon To Rinsho; 1980 Jul 15; 28(7):767-72. PubMed ID: 7460327
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  • 15. [Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype].
    Dzenis IG, Brykova EK, Bakharev VA.
    Akush Ginekol (Mosk); 1990 Jan 15; (1):10-4. PubMed ID: 2353725
    [No Abstract] [Full Text] [Related]

  • 16. Genetics of adrenal steroid 21-hydroxylase deficiency.
    New MI, Speiser PW.
    Endocr Rev; 1986 Aug 15; 7(3):331-49. PubMed ID: 3527688
    [Abstract] [Full Text] [Related]

  • 17. [Molecular genetic study of 21-hydroxylase deficiency gene conversion as a molecular mechanism of monogenic disorder].
    Harada F.
    Fukuoka Igaku Zasshi; 1987 Feb 15; 78(2):55-66. PubMed ID: 3495477
    [No Abstract] [Full Text] [Related]

  • 18. [Congenital adrenogenital syndrome].
    Knorr D.
    Monatsschr Kinderheilkd; 1985 Jun 15; 133(6):327-35. PubMed ID: 2931585
    [No Abstract] [Full Text] [Related]

  • 19. [New concepts in virilizing adrenal hyperplasia caused by 21-hydroxylase block].
    Cortínez A, Beas F, Devoto L, Henríquez C.
    Rev Chil Pediatr; 1985 Jun 15; 56(3):192-8. PubMed ID: 3879364
    [No Abstract] [Full Text] [Related]

  • 20. Preliminary investigation of mutations in 21-hydroxylase gene in patients with congenital adrenal hyperplasia in Russia.
    Evgrafov OV, Polyakov AV, Dzenis IG, Baharev VA.
    Hum Mutat; 1995 Jun 15; 5(2):131-6. PubMed ID: 7749411
    [Abstract] [Full Text] [Related]

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