Identification of type I collagen gene (COL1A2) mutations in nonlethal osteogenesis imperfecta

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Genotype and malocclusion in patients with osteogenesis imperfecta.

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Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2017

Molecular diagnosis in children with fractures but no extraskeletal signs of osteogenesis imperfecta.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2017

DNA sequence analysis in 598 individuals with a clinical diagnosis of osteogenesis imperfecta: diagnostic yield and mutation spectrum.

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