Resultados da busca - Majid Fardaei

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome por Maryam Taghdiri, Maryam Taghdiri, Hassan Dastsooz, Majid Fardaei, Majid Fardaei, Majid Fardaei, Sanaz Mohammadi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi

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Commentary: Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing por Mohammad Reza Heydari, Majid Fardaei

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Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports por Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, Majid Fardaei, Mohammad Ali Faghihi

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Clinical and genetic-epignetic aspects of recurrent hydatidiform mole: A review of literature por Najmeh Moein-Vaziri, Jafar Fallahi, Bahia Namavar-Jahromi, Majid Fardaei, Mozhdeh Momtahan, Zahra Anvar

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An immunocompetent patient with a nonsense mutation in NHEJ1 gene por Hossein Esmaeilzadeh, Mohammad Reza Bordbar, Zahra Hojaji, Parham Habibzadeh, Dorna Afshinfar, Mohammad Miryounesi, Majid Fardaei, Mohammad Ali Faghihi

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