Related Articles

• Beyond brittle bones: Genetic mechanisms underlying osteogenesis imperfecta (Review)
• A novel variant of osteogenesis imperfecta type IV and low serum phosphorus level caused by a Val94Asp mutation in COL1A1
• Application of next‑generation sequencing for molecular diagnosis in a large family with osteogenesis imperfecta type I
• Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfecta
• A novel mild variant of osteogenesis imperfecta type I caused by a Gly1088Glu mutation in COL1A1