Prevalence and natural course of craniocervical junction anomalies during growth in patients with osteogenesis imperfecta

Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta

(2011) Jutta Becker et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Zoledronic Acid Treatment in Children with Osteogenesis Imperfecta

(2011) Ilkka Vuorimies et al.   Hormone Research in Paediatrics

Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes

(2011) Shawna M. Pyott et al.   HUMAN MOLECULAR GENETICS

Mutations in SERPINF1 cause osteogenesis imperfecta type VI

(2011) Erica P Homan et al.   JOURNAL OF BONE AND MINERAL RESEARCH

New perspectives on osteogenesis imperfecta

(2011) Antonella Forlino et al.   Nature Reviews Endocrinology

Cranial base abnormalities in osteogenesis imperfecta: Phenotypic and genotypic determinants

(2010) Moira S Cheung et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Dimensions of the craniocervical junction in longitudinal analysis of normal growth

(2009) Heidi Arponen et al.   CHILDS NERVOUS SYSTEM

Classification of Osteogenesis Imperfecta revisited

(2009) F.S. Van Dijk et al.   European Journal of Medical Genetics

Specific entities affecting the craniocervical region

(2008) Arnold H. Menezes   CHILDS NERVOUS SYSTEM

Reliability of cranial base measurements on lateral skull radiographs

(2008) H Arponen et al.   Orthodontics & Craniofacial Research