Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas by Akbaroghli S, Balali M, Kamalidehghan B, Saber S, Aryani O, Yong Meng G, Houshmand M

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Association of genetic variations in the mitochondrial DNA control region with presbycusis by Falah M, Farhadi M, Kamrava SK, Mahmoudian S, Daneshi A, Balali M, Asghari A, Houshmand M

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The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis by Falah M, Houshmand M, Najafi M, Balali M, Mahmoudian S, Asghari A, Emamdjomeh H, Farhadi M

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Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss by Balali M, Kamalidehghan B, Farhadi M, Ahmadipour F, Ashkezari MD, Hemami MR, Arabzadeh H, Falah M, Meng GY, Houshm, M

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Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss by Balali, M., Kamalidehghan, B., Farhadi, M., Ahmadipour, F., Ashkezari, M.D., Hemami, M.R., Arabzadeh, H., Falah, M., Meng, G.Y., Houshmand, M.