Search Results - Mostofinezhad, Nioosha

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    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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  2. 2
    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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