Works matching IS 22285806 AND DT 2019 AND VI 21 AND IP 3


Results: 17
    1
    2
    3

    Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.

    Published in:
    Cell Journal (Yakhteh), 2019, v. 21, n. 3, p. 337, doi. 10.22074/cellj.2019.6053
    By:
    • Mohammadzadeh, Akbar;
    • Akbaroghli, Susan;
    • Aghaei-Moghadam, Ehsan;
    • Mahdieh, Nejat;
    • Badv, Reza Shervin;
    • Jamali, Payman;
    • Kariminejad, Roxana;
    • Chavoshzadeh, Zahra;
    • Firouzabadi, Saghar Ghasemi;
    • Ghanaie, Roxana Mansour;
    • Nozari, Ahoura;
    • Banihashemi, Sussan;
    • Hadipour, Fatemeh;
    • Hadipour, Zahra;
    • Kariminejad, Ariana;
    • Najmabadi, Hossein;
    • Shafeghati, Yousef;
    • Behjati, Farkhondeh
    Publication type:
    Article
    4
    5
    6
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17