F. Atalar Et Al. , "Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods," VI. Ulusal Tibbi Genetik Kongresi , Antalya, Turkey, pp.53, 2004
Atalar, F. Et Al. 2004. Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods. VI. Ulusal Tibbi Genetik Kongresi , (Antalya, Turkey), 53.
Atalar, F., Tükel, T., Yüksel Apak, M., Uyguner, O., Kayserili, H., & Wollnik, B., (2004). Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods . VI. Ulusal Tibbi Genetik Kongresi (pp.53). Antalya, Turkey
Atalar, Fatmahan Et Al. "Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods," VI. Ulusal Tibbi Genetik Kongresi, Antalya, Turkey, 2004
Atalar, Fatmahan Et Al. "Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods." VI. Ulusal Tibbi Genetik Kongresi , Antalya, Turkey, pp.53, 2004
Atalar, F. Et Al. (2004) . "Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods." VI. Ulusal Tibbi Genetik Kongresi , Antalya, Turkey, p.53.
@conferencepaper{conferencepaper, author={Fatmahan ATALAR Et Al. }, title={Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods}, congress name={VI. Ulusal Tibbi Genetik Kongresi}, city={Antalya}, country={Turkey}, year={2004}, pages={53} }