Treffer 1 - 5 von 5 für Suche 'Mazrouei, Bahareh', Suchdauer: 0,76s Treffer weiter einschränken
  1. 1
    Analysis of Missense Mutations of CX3CR1 Gene in Patients with Recurrent Pregnancy Loss Using Bioinformatics Tools

    Analysis of Missense Mutations of CX3CR1 Gene in Patients with Recurrent Pregnancy Loss Using Bioinformatics Tools von Mazrouei, Bahareh, Heidari, Mohammad Mehdi, Khatami, Mehri


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  2. 2
    Review of Genetic Changes and Factors Causing Cardiac Arrhythmias

    Review of Genetic Changes and Factors Causing Cardiac Arrhythmias von Khatami, Mehri, Heidari, Mohammad Mehdi, Mazrouei, Bahareh, Aflaki, Rojin


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  3. 3
    Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease

    Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease von Heidari, Mohammad Mehdi, Khatami, Mehri, Kamalipour, Akram, Kalantari, Mustafa, Movahed, Mahsa, Emmamy, Mohammad Hayet, Hadadzadeh, Mehdi, Bragança, José, Namnabat, Mohsen, Mazrouei, Bahareh

    Veröffentlicht in EXCLI journal

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  4. 4
    Molecular Mechanisms of Recurrent Pregnancy Loss

    Molecular Mechanisms of Recurrent Pregnancy Loss von Mazrouei, Bahareh, Heidari, Mohammad Mehdi, Khatami, Mehri, Tahmasebi, Maryam


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  5. 5
    Novel nucleotide variations in the thrombomodulin (THBD) gene involved in coagulation pathways can increase the risk of recurrent pregnancy loss (RPL)

    Novel nucleotide variations in the thrombomodulin (THBD) gene involved in coagulation pathways can increase the risk of recurrent pregnancy loss (RPL) von Heidari, Mohammad Mehdi, Mazrouei, Bahareh, Tahmasebi, Maryam, Bagheri, Fatemeh, Khanjankhani, Zahra, Khatami, Mehri, Dehghani, Mohammadreza, Khormizi, Fateme Zare

    Veröffentlicht in Gene

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