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2022 - 2017
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Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss
Fetal and pediatric pathology
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Thiol-disulfide homeostasis, serum ferroxidase activity, and serum ischemia modified albumin levels in neonatal jaundice
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