Search Results - Nasseri, Mojila

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  1. 1
    B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies

    B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycan... by Maroofian, Reza, Riemersma, Moniek, Jae, Lucas T, Zhianabed, Narges, Willemsen, Marjolein H, Wissink-Lindhout, Willemijn M, Willemsen, Michèl A, de Brouwer, Arjan P M, Mehrjardi, Mohammad Yahya Vahidi, Ashrafi, Mahmoud Reza, Kusters, Benno, Kleefstra, Tjitske, Jamshidi, Yalda, Nasseri, Mojila, Pfundt, Rolph, Brummelkamp, Thijn R, Abbaszadegan, Mohammad Reza, Lefeber, Dirk J, van Bokhoven, Hans

    Published in Genome medicine
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  2. 2
    Inherited genetic markers for thrombophilia in northeastern Iran (a clinical-based report)

    Inherited genetic markers for thrombophilia in northeastern Iran (a clinical-based report) by Keify, Fatemeh, Azimi-Nezhad, Mohsen, Zhiyan-Abed, Narges, Nasseri, Mojila, Abbaszadegan, Mohammad Reza

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  3. 3
    Frequency of Inborn Errors of Metabolism in a Northeastern Iranian Sample with High Consanguinity Rates

    Frequency of Inborn Errors of Metabolism in a Northeastern Iranian Sample with High Consanguinity Rates by Keyfi, Fatemeh, Nasseri, Mojila, Nayerabadi, Samira, Alaei, Amin, Mokhtariye, Armin, Varasteh, Abdolreza

    Published in Human heredity
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  4. 4
    Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia

    Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia by Kariminejad, Ariana, Szenker-Ravi, Emmanuelle, Lekszas, Caroline, Tajsharghi, Homa, Moslemi, Ali-Reza, Naert, Thomas, Tran, Hong Thi, Ahangari, Fatemeh, Rajaei, Minoo, Nasseri, Mojila, Haaf, Thomas, Azad, Afrooz, Superti-Furga, Andrea, Maroofian, Reza, Ghaderi-Sohi, Siavash, Najmabadi, Hossein, Abbaszadegan, Mohammad Reza, Vleminckx, Kris, Nikuei, Pooneh, Reversade, Bruno

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  5. 5
    Examining the Frequency of the JAK2 (V617F) Mutation in Patients with Myeloproliferative Diseases in North Eastern Iran and the Effect of Treatment Intervention

    Examining the Frequency of the JAK2 (V617F) Mutation in Patients with Myeloproliferative Diseases in North Eastern Iran and the Effect of Treatment Intervention by Nasseri, Mojila, Keyfi, Fatemeh, Rahbarian, Raheleh, Rajabian, Majid, Abbaszadegan, Mohammad Reza

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  6. 6
    The relationship between MTHFR polymorphisms and abortion in Iranian women

    The relationship between MTHFR polymorphisms and abortion in Iranian women by Keyfi, Fatemeh, Ebrahimzadeh-Vesal, Reza, Zhiyan, Narges, Nayebi, Minoo, Nasseri, Mojila, Abbaszadegan, Mohammad Reza

    Published in Gene reports
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