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Results: 1-3 |
Results: 3
CYP21 mutations in simple virilizing congenital adrenal hyperplasia
Authors: Lajic, S Robins, T Krone, N Schwarz, HP Wedell, A
Citation: S. Lajic et al., CYP21 mutations in simple virilizing congenital adrenal hyperplasia, J MOL MED-J, 79(10), 2001, pp. 581-586
Mothers with congenital adrenal hyperplasia and their children: outcome ofpregnancy, birth and childhood
Authors: Krone, N Wachter, I Stefanidou, M Roscher, AA Schwarz, HP
Citation: N. Krone et al., Mothers with congenital adrenal hyperplasia and their children: outcome ofpregnancy, birth and childhood, CLIN ENDOCR, 55(4), 2001, pp. 523-529
Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany
Authors: Krone, N Braun, A Roscher, AA Knorr, D Schwarz, HP
Citation: N. Krone et al., Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany, J CLIN END, 85(3), 2000, pp. 1059-1065
Risultati: 1-3 |