Search Results - Hoseininasab, Fatemeh

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  1. 1
    Whole exome sequencing identifies novel pathogenic variants in TGM1 and ALOX12B in patients with hereditary ichthyosis

    Whole exome sequencing identifies novel pathogenic variants in TGM1 and ALOX12B in patients with hereditary ichthyosis by Chegini, Mitra, Eslami, Maryam, Motavaf, Mahsa, Memarsadeghi, Omid, Hoseini, Azadeh, Torab, Elnaz, Hoseininasab, Fatemeh, Amiri, Hosna, Ramandi, Somayeh, Mostofinezhad, Niusha, Keivani, Fatane, Ghaffari, Saeed Reza, Rafati, Maryam

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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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  3. 3
    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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  4. 4
    Identification of a novel ALMS1 pathogenic variant in a family with Cone-Rod Dystrophy using whole exome sequencing, followed by prenatal diagnosis

    Identification of a novel ALMS1 pathogenic variant in a family with Cone-Rod Dystrophy using whole exome sequencing, followed by prenatal diagnosis by Rafati, Maryam, Tara, Seyedeh Zahra, Hoseininasab, Fatemeh, Ghaffari, Saeed Reza

    Published in Meta Gene
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  5. 5
    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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  6. 6
    Multisystem inflammatory syndrome in children (MIS-C) post-COVID-19 in Iran: clinical profile, cardiac features, and outcomes

    Multisystem inflammatory syndrome in children (MIS-C) post-COVID-19 in Iran: clinical profile, cardiac features, and outcomes by Hoseininasab, Ali, Sinaei, Reza, Bagheri, Mohammad Mehdi, Ahmadipour, Maryam, Derakhshan, Reza, Najafzadeh, Mohammad Javad, Robati, Fatemeh Karami, Jafari, Maedeh, Ebrahimi, Sarehossadat, Jafari, Mohammad Ali

    Published in BMC pediatrics
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