Clinical and radiographic delineation of odontochondrodysplasia

American Journal of Medical Genetics, Part A

Volumn 146, Issue 6, 2008, Pages 770-778

  Unger, Sheila ^a   Antoniazzi, Franco ^b   Brugnara, Milena ^b   Alanay, Yasemin ^c   Caglayan, Ahmet ^d   Lachlan, Katherine ^e   Ikegawa, Shiro ^f   Nishimura, Gen ^g   Zabel, Bernhard ^a   Spranger, Jürgen ^a   Superti Furga, Andrea ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

^b UNIVERSITY OF VERONA   (Italy)

^c HACETTEPE UNIVERSITY   (Turkey)

^d ERCIYES UNIVERSITY MEDICAL FACULTY   (Turkey)

^e PRINCESS ANNE HOSPITAL   (United Kingdom)

^f RIKEN   (Japan)

^g TOKYO METROPOLITAN CHILDREN'S MEDICAL CENTER   (Japan)

Author keywords

Dentinogenesis imperfecta (DI); Goldblatt syndrome; Odontochondrodysplasia (ODCD); Spondylometaphyseal dysplasia

Indexed keywords

COLLAGEN TYPE 2; FIBROBLAST GROWTH FACTOR RECEPTOR 3;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BONE DYSPLASIA; BONE MALFORMATION; BONE RADIOGRAPHY; CHILD; CHONDRODYSPLASIA; CLINICAL ARTICLE; CLINICAL FEATURE; COL2A1 GENE; COMP GENE; FEMALE; FGFR3 GENE; GENE; GOLDBLATT SYNDROME; HUMAN; INFANT; JOINT LAXITY; MALE; METAPHYSIS; ODONTOCHONDRODYSPLASIA; PLATYSPONDYLY; PRIORITY JOURNAL; RMRP GENE; SBDS GENE; SCOLIOSIS; SHORT STATURE; TOOTH MALFORMATION; VALGUS DEFORMITY;

ADOLESCENT; BONE AND BONES; CHILD, PRESCHOOL; FEMALE; HAND; HUMANS; INFANT; LOWER EXTREMITY; MALE; ODONTODYSPLASIA; OSTEOCHONDRODYSPLASIAS; PELVIS;

EID: 40449140398     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32214     Document Type: Article

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