Found: 2

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  • Effect of inbreeding on intellectual disability revisited by trio sequencing.

    Published in:
    Clinical Genetics, 2019, v. 95, n. 1, p. 151, doi. 10.1111/cge.13463
    By:
    • Kahrizi, Kimia;
    • Hosseini, Masoumeh;
    • Fattahi, Zohreh;
    • Beheshtian, Maryam;
    • Mohseni, Marzieh;
    • Mehvari, Sepideh;
    • Mehrjoo, Zohreh;
    • Akhtarkhavari, Tara;
    • Ghaderi, Zhila;
    • Rahimi, Maryam;
    • Arzhangi, Sanaz;
    • Falahat Chian, Milad;
    • Sadeghinia, Farnaz;
    • Najmabadi, Hossein;
    • Pourfatemi, Fatemeh;
    • Mojahedi, Faezeh;
    • Khodaie‐Ardakani, Mohammad‐Reza;
    • Najafipour, Reza;
    • Hu, Hao;
    • Kalscheuer, Vera M.
    Publication type:
    Article

  • Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum.

    Published in:
    Archives of Iranian Medicine (AIM), 2020, v. 23, n. 7, p. 426, doi. 10.34172/aim.2020.39
    By:
    • Taghizadeh, Sara;
    • Vazehan, Raheleh;
    • Beheshtian, Maryam;
    • Sadeghinia, Farnaz;
    • Fattahi, Zohreh;
    • Mohseni, Marzieh;
    • Arzhangi, Sanaz;
    • Nafissi, Shahriar;
    • Kariminejad, Ariana;
    • Najmabadi, Hossein;
    • Kahrizi, Kimia
    Publication type:
    Article