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A novel P3H1 mutation is associated with osteogenesis imperfecta type VIII and dental anomalies.
Phenotypic Variation in Vietnamese Osteogenesis Imperfecta Patients Sharing a Recessive P3H1 Pathoge…
Severe cases of osteogenesis imperfecta type VIII due to a homozygous mutation in P3H1 (LEPRE1) and …
A new case of osteogenesis imperfecta type VIII and retinal detachment.
Osteogenesis Imperfecta: Search for Mutations in Patients from the Republic of Bashkortostan (Russia…
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Urinary Biomarkers of OI Pathobiology
Safety of Fresolimumab in the Treatment of Osteogenesis Imperfecta
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