Items where Author is "Kolahdouz, P."
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(2018) A Rare Missense Mutation and a Polymorphism with High Frequency in LDLR Gene among Iranian Patients with Familial Hypercholesterolemia. Adv Biomed Res. p. 37. ISSN 2277-9175 (Print) 2277-9175 (Linking)
(2015) Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia. Advanced biomedical research. p. 189. ISSN 2277-9175 (Print) 2277-9175 (Linking)