Advanced Biomedical Research
Author = Kolahdouz, Parisa
Number of Articles: 2
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
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