Keywords = 21-hydroxylase deficiency
Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche

Volume 2016, March, March 2016, Pages 1-4

Mahsa Kolahdouz; Mahin Hashemipour; Hossein Khanahmad; Bahareh Rabbani; Mansoor Salehi; Ali Rabbani; Mona Mobalegh Naseri


Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia

Volume 2015, August, August 2015, Pages 1-5

Mahsa Kolahdouz; Zahra Mohammadi; Parisa Kolahdouz; Masoud Tajamolian; Hossein Khanahmad