B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies
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 (22.12.2017)
Published in Genome medicine (22.12.2017)
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Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia
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
Published in American journal of human genetics (05.12.2019)
Published in American journal of human genetics (05.12.2019)
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Examining the Frequency of the JAK2 (V617F) Mutation in Patients with Myeloproliferative Diseases in North Eastern Iran and the Effect of Treatment Intervention
Nasseri, Mojila, Keyfi, Fatemeh, Rahbarian, Raheleh, Rajabian, Majid, Abbaszadegan, Mohammad Reza
Published in Reports of biochemistry and molecular biology (01.07.2020)
Published in Reports of biochemistry and molecular biology (01.07.2020)
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The relationship between MTHFR polymorphisms and abortion in Iranian women
Keyfi, Fatemeh, Ebrahimzadeh-Vesal, Reza, Zhiyan, Narges, Nayebi, Minoo, Nasseri, Mojila, Abbaszadegan, Mohammad Reza
Published in Gene reports (01.12.2018)
Published in Gene reports (01.12.2018)
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