Showing 1 - 2 results of 2 for search 'Mehdi Agha Gholizadeh', query time: 0.01s Refine Results
  1. 1
    A Novel Frameshift Mutation in Abnormal Spindle-Like Microcephaly (ASPM) Gene in an Iranian Patient with Primary Microcephaly: A Case Report

    A Novel Frameshift Mutation in Abnormal Spindle-Like Microcephaly (ASPM) Gene in an Iranian Patient with Primary Microcephaly: A Case Report by Afsaneh BAZGIR, Mehdi AGHA GHOLIZADEH, Faezeh SARVAR, Zahra PAKZAD

    Published 2019
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  2. 2
    Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the PRUNE1 gene

    Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the... by Mehdi Agha Gholizadeh, Mina Mohammadi-Sarband, Fatemeh Fardanesh, Masoud Garshasbi

    Published 2022
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