Related references
Note: Only part of the references are listed.Osteogenesis Imperfecta Type III With Intracranial Hemorrhage and Brachydactyly Associated With Mutations in Exon 49 of COL1A2
Eissa Faqeih et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)
Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships
Dale L. Bodian et al.
HUMAN MOLECULAR GENETICS (2009)
Evidence that abnormal high bone mineralization in growing children with osteogenesis imperfecta is not associated with specific collagen mutations
Paul Roschger et al.
CALCIFIED TISSUE INTERNATIONAL (2008)
Consortium for osteogeneslis imperfecta mutations in the helical domain of type I collagen: Regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans
Joan C. Marini et al.
HUMAN MUTATION (2007)
Osteogenesis imperfecta:: clinical, biochemical and molecular findings
G. Venturi et al.
CLINICAL GENETICS (2006)
Centers for Disease Control and Prevention 2000 growth charts for the United States: Improvements to the 1977 National Center for Health Statistics version
CL Ogden et al.
PEDIATRICS (2002)
Share Paper
