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Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome.
Nasiri J, Salehi M, Hosseinzadeh M, Zamani M, Fattahpour S, Aryani O, Fazel Najafabadi E, Jabarzadeh M, Asadi S, Gholamrezapour T, Sedghi M, Ghorbani F. Nasiri J, et al. Among authors: sedghi m. Iran J Child Neurol. 2019 Summer;13(3):25-34. Iran J Child Neurol. 2019. PMID: 31327966 Free PMC article.
Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset.
Nouri N, Fazel-Najafabadi E, Salehi M, Hosseinzadeh M, Behnam M, Ghazavi MR, Sedghi M. Nouri N, et al. Among authors: sedghi m. Adv Biomed Res. 2014 Jan 27;3:72. doi: 10.4103/2277-9175.125862. eCollection 2014. Adv Biomed Res. 2014. PMID: 24627880 Free PMC article.
91 results