Search Results - Mohamadhashem, Faezeh

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  1. 1
    PTGS2 (COX2) −765G>C gene polymorphism and risk of sporadic colorectal cancer in Iranian population

    PTGS2 (COX2) −765G>C gene polymorphism and risk of sporadic colorectal cancer in Iranian population by Daraei, Abdolreza, Salehi, Rasoul, Mohamadhashem, Faezeh

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  2. 2
    DNA-methyltransferase 3B 39179 G > T polymorphism and risk of sporadic colorectal cancer in a subset of Iranian population

    DNA-methyltransferase 3B 39179 G > T polymorphism and risk of sporadic colorectal cancer in a subset of Iranian population by Daraei, Abdolreza, Salehi, Rasul, MohamadHashem, Faezeh

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  3. 3
    Virtual Screening and Pharmacophore Design for a Novel Theoretical Inhibitor of Macrophage Stimulating Factor as a Metastatic Agent

    Virtual Screening and Pharmacophore Design for a Novel Theoretical Inhibitor of Macrophage Stimulating Factor as a Metastatic Agent by Torktaz, Ibrahim, Mohamadhashem, Faezeh, Esmaeili, Abolghasem, Behjati, Mohaddeseh, Sharifzadeh, Sara

    Published in Bioimpacts
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  4. 4
    Identification of a novel de novo variant in OTX2 in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosis

    Identification of a novel de novo variant in OTX2 in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosis by Rafati, Maryam, Mohamadhashem, Faezeh, Jalilian, Koosha, Hoseininasab, Fatemeh, Fakhri, Laya, Hoseini, Azadeh, Amiri, Hosna, Barati, Zeinab, Darzi Ramandi, Somayeh, Mostofinezhad, Nioosha, Mahmoudi, Amir Hosein, Ghaffari, Saeed Reza

    Published in Ophthalmic genetics
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  5. 5
    A novel ACVR1 mutation detected by whole exome sequencing in a family with an unusual skeletal dysplasia

    A novel ACVR1 mutation detected by whole exome sequencing in a family with an unusual skeletal dysplasia by Rafati, Maryam, Mohamadhashem, Faezeh, Hoseini, Azadeh, Hoseininasab, Fatemeh, RezaGhaffari, Saeed

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  6. 6
    Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation Sequencing

    Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation Sequencing by Rafati, Maryam, Mohamadhashem, Faezeh, Hoseini, Azadeh, Ramandi, Somayeh Darzi, Ghaffari, Saeed Reza

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  7. 7
    Identification of a novel de novo variant in OTX2 in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosis

    Identification of a novel de novo variant in OTX2 in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosis by Rafati, Maryam, Mohamadhashem, Faezeh, Jalilian, Koosha, Hoseininasab, Fatemeh, Fakhri, Laya, Hoseini, Azadeh, Amiri, Hosna, Barati, Zeinab, Darzi Ramandi, Somayeh, Mostofinezhad, Nioosha, Mahmoudi, Amir Hosein, Ghaffari, Saeed Reza

    Published in Ophthalmic Genetics
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