Clinical outcome and genotype in patients with hereditary multiple exostoses

Journal of Orthopaedic Research

Volumn 25, Issue 12, 2007, Pages 1541-1551

  Jäger, Marcus ^a,b   Westhoff, Bettina ^a   Portier, Sebastian ^a   Leube, Barbara ^a   Hardt, Karin ^a   Royer Pokora, Brigitte ^a   Goßheger, Georg ^c   Krauspe, Rüdiger ^a  

^a UNIVERSITY HOSPITAL DÜSSELDORF   (Germany)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c INST OF REPRO MED OF THE UNIV   (Germany)

Author keywords

EXT genes; Genotype phenotype; Hereditary multiple exostoses; Linkage exclusion analysis

Indexed keywords

ADOLESCENT; ADULT; ANAMNESIS; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BONE RADIOGRAPHY; CHILD; CLINICAL EXAMINATION; CLINICAL FEATURE; DISEASE SEVERITY; FEMALE; FOLLOW UP; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CORRELATION; GENETIC LINKAGE; GENETIC RISK; GENOTYPE PHENOTYPE CORRELATION; HEREDITARY MULTIPLE EXOSTOSIS; HUMAN; INFANT; LEG LENGTH; LINKAGE ANALYSIS; MALE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGE FACTORS; BONE AND BONES; CHILD; CHILD, PRESCHOOL; EXOSTOSES, MULTIPLE HEREDITARY; FEMALE; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; MALE; N-ACETYLGLUCOSAMINYLTRANSFERASES; PHENOTYPE; PROSPECTIVE STUDIES; SEX FACTORS;

EID: 37349096977     PISSN: 07360266     EISSN: None     Source Type: Journal    
DOI: 10.1002/jor.20479     Document Type: Article

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