Type II collagenopathies: Are there additional family members?

American Journal of Medical Genetics

Volumn 63, Issue 1, 1996, Pages 137-143

  Freisinger, P ^a   Bonaventure, J ^d   Stoess, H ^c   Pontz, B F ^a   Emmrich, P ^a   Nerlich, A ^b  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

^c Pathologisches Institut   (Germany)

^d HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

chondrodysplasia; Kniest dysplasia; platyspondylic dysplasia, Torrance type; type II collagenopathies

Indexed keywords

COLLAGEN TYPE 2;

ARTICLE; CHONDRODYSPLASIA; CLINICAL FEATURE; COLLAGEN DISEASE; COLLAGEN SYNTHESIS; EPIPHYSEAL CARTILAGE; GENE EXPRESSION; GENE MAPPING; GENETIC CODE; HUMAN; HUMAN TISSUE; LETHAL GENE; PRIORITY JOURNAL;

BONE AND BONES; BONE DEVELOPMENT; COLLAGEN; COLLAGEN DISEASES; FEMALE; GROWTH PLATE; HUMANS; INFANT, NEWBORN; MALE; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 0029968237     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960503)63:1<137::AID-AJMG24>3.0.CO;2-O     Document Type: Article

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