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Dardis, A
Marino, R
Bergada, I
Escobar, ME
Gryngarten, M
Rivarola, MA
Belgorosky, A
Citation: A. Dardis et al., Molecular analysis of the most frequent mutations associated with congenital adrenal hyperplasia secondary to steroid 21-hydroxylase enzyme deficiency, MEDICINA, 61(1), 2001, pp. 28-34
Authors:
Dardis, A
Saraco, N
Rivarola, MA
Belgorosky, A
Citation: A. Dardis et al., Decrease in the expression of the 3 beta-hydroxysteroid dehydrogenase genein human adrenal tissue during prepuberty and early puberty: Implications for the mechanism of adrenarche, PEDIAT RES, 45(3), 1999, pp. 384-388
Authors:
Dardis, A
Saraco, N
Berensztein, E
Rivarola, M
Belgorosky, A
Citation: A. Dardis et al., Role of 3 beta hydroxysteroid dehydrogenase (3 beta HSD) in human adrenal androgen synthesis., MEDICINA, 59(1), 1999, pp. 79-82
Authors:
Wijesuriya, SD
Zhang, GR
Dardis, A
Miller, WL
Citation: Sd. Wijesuriya et al., Transcriptional regulatory elements of the human gene for cytochrome P450c21 (steroid 21-hydroxylase) lie within intron 35 of the linked C4B gene, J BIOL CHEM, 274(53), 1999, pp. 38097-38106