Idézéskapcsolat

Krnić Nevena. Kliničke, biokemijske i molekularne karakteristike bolesnika s neklasičnom kongenitalnom adrenalnom hiperplazijom zbog manjka 21-hidroksilaze [Clinical, biochemical and molecular characteristics of the patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency]. (2014)

Közlemény:
Patócs A et al. Hormonal evaluation and mutation screening for steroid 21-hydrosylase deficiency in patients with unilateral and bilateral adrenal incidentalomas. (2002) EUROPEAN JOURNAL OF ENDOCRINOLOGY 0804-4643 1479-683X 147 3 349-355
Idéző közlemény:
Krnić Nevena. Kliničke, biokemijske i molekularne karakteristike bolesnika s neklasičnom kongenitalnom adrenalnom hiperplazijom zbog manjka 21-hidroksilaze [Clinical, biochemical and molecular characteristics of the patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency]. (2014)
Független: Igen
2021-05-17 14:18