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Results: 1-3 |
Results: 3

Authors: 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: Gryngarten, M Bedecarras, P Ayuso, S Bergada, C Campo, S Escobar, ME
Citation: M. Gryngarten et al., Clinical assessment and serum hormonal profile in prepubertal hypertrichosis, HORMONE RES, 54(1), 2000, pp. 20-25

Authors: Bedecarras, P Gryngarten, M Ayuso, S Escobar, ME Bergada, C Campo, S
Citation: P. Bedecarras et al., Characterization of serum SHBG isoforms in prepubertal and pubertal girls, CLIN ENDOCR, 49(5), 1998, pp. 603-608
Risultati: 1-3 |