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Madrimova A.G

4 ta ish

Toshkent davlat tibbiyot universiteti

AkademScholarda batafsil koʻrsatkichlar

  1. MITOCHONDRIAL MUTATION m.1555A>G IN MT-RNR1 AS A PREDICTIVE BIOMARKER OF AMINOGLYCOSIDE-INDUCED SENSORINEURAL HEARING LOSS IN CHILDREN

    Madrimova A.G

    MaqolaOchiq kirishNeonatal Respiratory Health ResearchZenodo (CERN European Organization for Nuclear Research)20260 iqtibos
    ABI

  2. MUTATIONAL SPECTRUM OF THE GJB2 GENE AS THE LEADING GENETIC CAUSE OF NON-SYNDROMIC SENSORINEURAL HEARING LOSS IN CHILDREN

    Madrimova A.G

    MaqolaHearing, Cochlea, Tinnitus, GeneticsZenodo (CERN European Organization for Nuclear Research)20260 iqtibos
    ABI

  3. MITOCHONDRIAL MUTATION m.1555A>G IN MT-RNR1 AS A PREDICTIVE BIOMARKER OF AMINOGLYCOSIDE-INDUCED SENSORINEURAL HEARING LOSS IN CHILDREN

    Madrimova A.G

    MaqolaNeonatal Respiratory Health ResearchZenodo (CERN European Organization for Nuclear Research)20260 iqtibos
    ABI

  4. MUTATIONAL SPECTRUM OF THE GJB2 GENE AS THE LEADING GENETIC CAUSE OF NON-SYNDROMIC SENSORINEURAL HEARING LOSS IN CHILDREN

    Madrimova A.G

    MaqolaOchiq kirishHearing, Cochlea, Tinnitus, GeneticsZenodo (CERN European Organization for Nuclear Research)20260 iqtibos
    ABI