Hasil Pencarian - Reza Pazhoomand

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  1. 1
    Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report

    Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report oleh Reza Mohammadi, Raheleh Taheri, Fatemeh Shahriyari, Farnaz Feiz, Zahra Mohammadi, Sadegh Shirian, Reza Raoofian, Abdorrasoul Malekpour, Reza Pazhoomand

    Diterbitkan 2021-05-01
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  2. 2
    TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia

    TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia oleh Mahsa Sadat Asl Mohajeri, Atieh Eslahi, Zeinab Khazaii, Mohammad Reza Moradi, Reza Pazhoomand, Shima Farrokhi, Masoumeh Heidari Feizabadi, Farzaneh Alizadeh, Majid Mojarrad

    Diterbitkan 2021-07-01
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  3. 3
    Haplotype diversity of 17 Y-STR in the Iranian population

    Haplotype diversity of 17 Y-STR in the Iranian population oleh Mohammad Reza Eskandarion, Arash Alipour Tabrizi, Reza Shirkoohi, Reza Raoofian, Masume Naji, Reza Pazhoomand, Hooman Salari, Bahram Samadirad, Alireza Sabouri, Mostafa Montazer Zohour, Hadi Namazi, Pegah Farhadi, Zohre Baratieh, Minoo Sayyari, Maliheh Dadgarmoghaddam, Esmat Safdarian, Afrooz Nikbakht, Farnaz Golshan, Fatemeh Baybordi, Elham Madhaji, Shadi ShohodiFar, Mohsen Tabasi, Ramezan Mohebbi

    Diterbitkan 2024-04-01
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