Search Results - Majid Fardaei
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1
A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome by Maryam Taghdiri, Maryam Taghdiri, Hassan Dastsooz, Majid Fardaei, Majid Fardaei, Majid Fardaei, Sanaz Mohammadi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi
Published 2017Call Number: Loading…Connect to this object online.
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2
Commentary: Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing by Mohammad Reza Heydari, Majid Fardaei
Published 2020Call Number: Loading…Connect to this object online.
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3
Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports by Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, Majid Fardaei, Mohammad Ali Faghihi
Published 2017Call Number: Loading…Connect to this object online.
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4
Clinical and genetic-epignetic aspects of recurrent hydatidiform mole: A review of literature by Najmeh Moein-Vaziri, Jafar Fallahi, Bahia Namavar-Jahromi, Majid Fardaei, Mozhdeh Momtahan, Zahra Anvar
Published 2018Call Number: Loading…Connect to this object online.
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5
An immunocompetent patient with a nonsense mutation in NHEJ1 gene by Hossein Esmaeilzadeh, Mohammad Reza Bordbar, Zahra Hojaji, Parham Habibzadeh, Dorna Afshinfar, Mohammad Miryounesi, Majid Fardaei, Mohammad Ali Faghihi
Published 2019Call Number: Loading…Connect to this object online.
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