Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods
Author
YÜKSEL APAK, MEMNUNE
WOLLNIK, B
Tükel, Turgut
UYGUNER, O
KAYSERILI, HÜLYA
ATALAR, Fatmahan
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