Idézéskapcsolat

Falhammar H et al. Biochemical and genetic diagnosis of 21-hydroxylase deficiency. (2015) ENDOCRINE 1355-008X 1559-0100 0969-711X 50 2 306-314

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 H et al. Biochemical and genetic diagnosis of 21-hydroxylase deficiency. (2015) ENDOCRINE 1355-008X 1559-0100 0969-711X 50 2 306-314
Független: Igen
2021-05-11 22:12