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Journal Abstract Search

114 related items for PubMed ID: 517053

  • 1. Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency confirmed by HLA tissue typing.
    Zachmann M, Prader A.
    Acta Endocrinol (Copenh); 1979 Nov; 92(3):542-6. PubMed ID: 517053
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  • 3. [Study of the transmission of the 21-hydroxylase deficiency through the hormonal screening and the HLA-typing (author's transl)].
    Bartolotta E, Migliori C, Gabrielli A, Oggiano N, Catassi C, Leone L.
    Pediatr Med Chir; 1981 Nov; 3(4):287-90. PubMed ID: 6283486
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  • 5. Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Zachmann M, Prader A.
    Acta Endocrinol (Copenh); 1978 Mar; 87(3):557-65. PubMed ID: 580145
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  • 6. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S, Levine LS, Lorenzen F, Chow D, Pollack M, Dupont B, Genel M, New MI.
    J Clin Endocrinol Metab; 1980 Mar; 50(3):586-9. PubMed ID: 6244328
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  • 7. Prenatal diagnosis of congenital adrenal hyperplasia.
    Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.
    Am J Med Genet; 1979 Mar; 4(2):201-4. PubMed ID: 517576
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  • 8. [Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype].
    Dumić M, Brkljacić L, Krzisnik C, Radica A, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 Mar; 105(7-8):290-2. PubMed ID: 6605467
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  • 10. 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 Mar; 200():243-55. PubMed ID: 3001775
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  • 12. Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.
    Laron Z, Pollack MS, Zamir R, Roitman A, Dickerman Z, Levine LS, Lorenzen F, O'Neill GJ, Pang S, New MI, Dupont B.
    Hum Immunol; 1980 Jul; 1(1):55-66. PubMed ID: 6266983
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  • 17. [Detection of heterozygosity in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the general population].
    Dumić M, Lukenda M, Plavsić V, Brkljacić L, Jovanović V, Kastelan A.
    Lijec Vjesn; 1990 Jul; 112(5-6):138-41. PubMed ID: 2172673
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