View Document Preview and Link Document Date: 2015-04-08 23:11:01 Open Document File Size: 619,91 KB Share Result on Facebook
Company Redbank / / Country Australia / / Currency USD / / / Facility The Children’s Hospital / Loading dock / / / IndustryTerm transportation / interpretation software / / MedicalCondition infectious risk / X-linked hypophosphataemic rickets / cataracts / Parallel Sequencing Bone Fragility Disorder / Vitamin D-dependent rickets / Bruck syndrome / adult Hypophosphatasia / SP7 Hereditary Rickets / Brittle Bone Disorders / Hypophosphatemic rickets / Hereditary Rickets / inherited disorders / disorder / XII Osteoporosis-pseudoglioma syndrome Osteopetrosis / hypercalciuria Dent disease Hypophosphatemic rickets Hypophosphatasia / Panel Brittle Bone Disorders / rickets / Osteogenesis imperfecta / childhood Hypophosphatasia / Email bruce.bennetts@health.nsw.gov.au Massively Parallel Sequencing Bone Fragility Disorder / XI Osteogenesis imperfecta / disorders / anophthalmia / / MedicalTreatment counselling / / Organization Department of Molecular Genetics / Department of Molecular Genetics Massively Parallel Sequencing for Brittle Bone Disorders and Hereditary Rickets Osteogenesis / AR AD / Department of Molecular Genetics Ph / Children’s Hospital / / / Position Governor / / Product BMP-1 / vitamin D / A280 / / Technology bioinformatics / gene targeting / / URL http / SocialTag 
Department of Molecular Genetics Massively Parallel Sequencing for Brittle Bone Disorders and Hereditary Rickets Osteogenesis imperfecta (OI) comprises a group of inherited disorders characterized by bone fragility and