Osteogenesis imperfecta type VI: A form of brittle bone disease with a mineralization defect

Journal of Bone and Mineral Research

Volumn 17, Issue 1, 2002, Pages 30-38

  Glorieux, Francis H ^a,b   Ward, Leanne M ^a   Rauch, Frank ^a,b   Lalic, Ljiljana ^a   Roughley, Peter J ^a,b   Travers, Rose ^a  

^a SHRINERS HOSPITAL FOR CHILDREN   (Canada)

^b MCGILL UNIVERSITY   (Canada)

Author keywords

Children; Histomorphometry; Osteogenesis imperfecta; Osteomalacia

Indexed keywords

COLLAGEN TYPE 1;

ADOLESCENT; ARTICLE; BONE DENSITY; BONE MINERALIZATION; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE CLASSIFICATION; DISEASE SEVERITY; ENZYME ASSAY; EXON; FEMALE; FRACTURE; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; HISTOPATHOLOGY; HUMAN; INHERITANCE; INTRON; MALE; MINERAL METABOLISM; MORPHOMETRICS; OSTEOGENESIS IMPERFECTA; PHENOTYPE; PROTEIN ANALYSIS; TOOTH DEVELOPMENT;

EID: 0036133709     PISSN: 08840431     EISSN: None     Source Type: Journal    
DOI: 10.1359/jbmr.2002.17.1.30     Document Type: Article

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