Hasil Pencarian - Balali M

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Perbaiki Hasil
  1. 1
    Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas

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

    Diterbitkan 2016-12-01
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  2. 2
    Association of genetic variations in the mitochondrial DNA control region with presbycusis

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

    Diterbitkan 2017-03-01
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  3. 3
    The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis

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

    Diterbitkan 2016-10-01
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  4. 4
    Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss

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

    Diterbitkan 2016-01-01
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