Author = Kolahdouz, Parisa
A Rare Missense Mutation and a Polymorphism with High Frequency in LDLR Gene among Iranian Patients with Familial Hypercholesterolemia

Volume 2018, February, February 2018, Pages 1-6

Masoud Tajamolian; Parisa Kolahdouz; Parvaneh Nikpour; Seyed Khalil Forouzannia; Mohammad Hasan Sheikhha; Ehsan Farashahi Yazd

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