Diagnosing osteogenesis imperfecta
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference11 articles.
1. Unexplained fractures in infancy: looking for fragile bones;Bishop;Arch Dis Child,2007
2. Genetic evaluation of suspected osteogenesis imperfecta (OI);Byers;Genet Med,2006
3. Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta;Cabral;Nat Genet,2007
4. Osteogenesis imperfecta: update on presentation and management;Cheung;Rev Endocr Metab Disord,2008
5. Type V osteogenesis imperfecta: a new form of brittle bone disease;Glorieux;J Bone Miner Res,2000
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