Idézéskapcsolat

Falhammar Henrik et al. Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: clinical presentation, diagnosis, treatment, and outcome. (2015) ENDOCRINE 1355-008X 1559-0100 0969-711X 50 1 32-50

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:
Falhammar Henrik et al. Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: clinical presentation, diagnosis, treatment, and outcome. (2015) ENDOCRINE 1355-008X 1559-0100 0969-711X 50 1 32-50
Független: Igen
2021-05-15 19:37