Found: 3
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21-Hydroxylase and 11β-hydroxylase mutations in Romanian patients with classic congenital adrenal hyperplasia.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Three New 46,XX Male Patients: A Clinical, Cytogenetic and Molecular Analysis.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2005, v. 18, n. 2, p. 197, doi. 10.1515/jpem.2005.18.2.197
- By:
- Publication type:
- Article
Mutational Analysis and Genotype-Phenotype Correlation in Patients with Classic 21-Hydroxylase Deficiency from Transylvania (North-West Romania).
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2002, v. 15, n. 9, p. 1505, doi. 10.1515/jpem.2002.15.9.1505
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- Publication type:
- Article