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Volumn 15, Issue 9, 2000, Pages 1650-1658

Type V osteogenesis imperfecta: A new form of brittle bone disease

(10) Glorieux, Francis H a,b Rauch, Frank a Plotkin, Horacio a Ward, Leanne a Travers, Rose a Roughley, Peter a,b Lalic, Ljiljana a Glorieux, Delphine F b Fassier, François b Bishop, Nicholas J a,c

a SHRINERS HOSPITAL FOR CHILDREN (Canada)

b MCGILL UNIVERSITY (Canada)

c UNIVERSITY OF SHEFFIELD (United Kingdom)

Author keywords

Autosomal dominant; Bone fragility; Children; Hyperplastic callus; Interosseous membrane; Osteogenesis imperfecta

Indexed keywords

GLYCINE;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE DENSITY; BONE METABOLISM; CALLUS; CLINICAL ARTICLE; CYTOGENETICS; DISEASE CLASSIFICATION; FEMALE; GENETIC DISORDER; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MORPHOMETRICS; OSTEOGENESIS IMPERFECTA; PHENOTYPE; SCORING SYSTEM; URINARY EXCRETION;

ADOLESCENT; ALKALINE PHOSPHATASE; BIOLOGICAL MARKERS; BIRTH WEIGHT; BODY WEIGHT; BONE AND BONES; BONE DENSITY; CHILD; CHILD, PRESCHOOL; FEMALE; FIBROBLASTS; GENES, DOMINANT; HUMANS; HYPERPLASIA; INFANT, NEWBORN; KARYOTYPING; MALE; MUTATION; OSTEOGENESIS IMPERFECTA; TERMINOLOGY;

EID: 0033848677 PISSN: 08840431 EISSN: None Source Type: Journal
DOI: 10.1359/jbmr.2000.15.9.1650 Document Type: Article

Times cited : (402)

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