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A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site by Ashkan Habib, Alireza Shojazadeh, Mohadeseh Molayemat, Hossein Jafari Khamirani, Sina Zoghi, Seyed Alireza Dastgheib, Asadollah Habib
Published 2021-07-01
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Prevalence and predictive factors of transient and permanent congenital hypothyroidism in Fars province, Iran by Ashkan Habib, Alireza Shojazadeh, Mohadeseh Molayemat, Asadollah Habib, Marjan Jeddi, Rita Arabsolghar, Mitra Nahas, Nazila Rahimi, Fariba Moradi Ardekani
Published 2021-06-01
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