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 by Talebi, Farah, Ghanbari Mardasi, Farideh, Javad, Mohammadi Asl, Amir Hooshang, Bavarsad, Masoumeh, Salehi Kambo

    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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    Journal Article
  2. 2

    Identification of a novel missence mutation in FGFR3 gene in an Iranian family with LADD syndrome by Next-Generation Sequencing by Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Bavarsad, Amir Hooshang, Tizno, Saeed

    “…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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    Journal Article
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