Search Results - "Bavarsad, Amir Hooshang"
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Next-Generation Sequencing Reveals One Novel Missense Mutation in COL1A2 Gene in an Iranian Family with Osteogenesis imperfecta
Published in Iranian biomedical journal (01-09-2017)“…Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous disorder characterized by bone loss and bone fragility. The aim of this study was to…”
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Identification of a novel missence mutation in FGFR3 gene in an Iranian family with LADD syndrome by Next-Generation Sequencing
Published in International journal of pediatric otorhinolaryngology (01-06-2017)“…Abstract Lacrimo-auriculo-dento-digital syndrome (LADD) is a multiple congenital anomaly and a genetically heterogeneous disorder. The aim of this study was to…”
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Prevalence and predictors of low back pain among the Iranian population: Results from the Persian cohort study
Published in Annals of medicine and surgery (01-02-2022)“…Low back pain (LBP) is a common health condition in populations. Limited large-scale population-based studies evaluated the prevalence and predictors of LBP in…”
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