Two questions about osteogenesis imperfecta

Journal of Pediatric Orthopaedics

Volumn 26, Issue 1, 2006, Pages 148-149

  Plotkin, Horacio ^a,b  

^a UNIVERSITY OF NEBRASKA AT OMAHA   (United States)

^b 985456 Nebraska Medical Center ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE DENSITY; BONE FRAGILITY; BONE MASS; CHILD; CHROMOSOME 17; CHROMOSOME 7; CLINICAL FEATURE; COL1A1 GENE; COL1A2 GENE; DISEASE SEVERITY; GENE; GENE LOCATION; GENE MUTATION; HUMAN; INFANT; OSTEOGENESIS IMPERFECTA; PHENOTYPE; PRIORITY JOURNAL; PROGNOSIS; SHORT SURVEY; ARTICLE; CHONDRODYSPLASIA; CLASSIFICATION; DIFFERENTIAL DIAGNOSIS; FEMALE; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETICS; MALE; NEWBORN; PEDIGREE; PRESCHOOL CHILD; RISK ASSESSMENT;

CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; INFANT; INFANT, NEWBORN; MALE; OSTEOCHONDRODYSPLASIAS; OSTEOGENESIS IMPERFECTA; PEDIGREE; PROGNOSIS; RISK ASSESSMENT;

EID: 33644866484     PISSN: 02716798     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.bpo.0000194697.21645.d3     Document Type: Short Survey

References (13)

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