Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods


Atalar F., Tükel T., Yüksel Apak M., Uyguner O., Kayserili H., Wollnik B.

VI. Ulusal Tibbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.53, (Full Text)

  • Publication Type: Conference Paper / Full Text
  • City: Antalya
  • Country: Turkey
  • Page Numbers: pp.53
  • Istanbul University Affiliated: Yes