TY  - JOUR
AU  - Rios Rodenas, Mercedes
AU  - Nova García, Manuel Joaquín De
AU  - Gutiérrez Díez, Mª Pilar
AU  - Feijoo García, Gonzalo
AU  - Mourelle Martínez, Rosa
AU  - Garcilazo Ambriz, Mario
AU  - Ortega Aranegui, Ricardo
PY  - 2015
DO  - 10.4317/jced.52126
SN  - 1988-8708
UR  - https://hdl.handle.net/20.500.14352/102215
T2  - Journal of Clinical Experimental Dentistry
AB  - Osteogenesis imperfecta (OI) is a hereditary bone fragility disorder that in most patients is caused by mutations affecting collagen type I. Their typical oral and craneofacial characteristics (Dentinogenesis imperfecta type I and class III...
LA  - eng
M2  - e153
PB  - Medicina Oral
KW  - osteogenesis imperfecta
KW  - craniovertebral junction
KW  - cephalometric
TI  - A cephalometric method to diagnosis the craniovertebral junction abnormalities in osteogenesis imperfecta patients
TY  - journal article
VL  - 7
ER  -