Dentinogenesis imperfecta-associated syndromes
- 25 September 2001
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 104 (1) , 75-78
- https://doi.org/10.1002/ajmg.10031
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Discrimination of morphological findings in dentine from osteogenesis imperfecta patients using combinations of polarized light microscopy, microradiograhpy and scanning electron microscopyInternational Journal of Paediatric Dentistry, 1999
- Scanning electron microscopy of teeth in osteogenesis imperfecta type IOral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology, 1996
- Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxityAmerican Journal of Medical Genetics, 1992
- Unique dwarfing, spondylometaphyseal skeletal dysplasia, with joint laxity and dentinogenesis imperfectaAmerican Journal of Medical Genetics, 1991
- A Polish variant of isolated dentinogenesis imperfecta with a generalised connective tissue defectBritish Dental Journal, 1989
- Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfectaClinical Genetics, 1989
- The Dentition in the Osteogenesis Imperfecta SyndromesPublished by Wolters Kluwer Health ,1981
- Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: another type of osteogenesis imperfecta?Journal of Medical Genetics, 1981
- Immunohistochemical localization of Type III collagen in the dentin of patients with osteogenesis imperfecta and hereditary opalescent dentinJournal of Oral Pathology & Medicine, 1980
- Scanning electron microscopy of teeth in dominant osteogenesis imperfecta: Support for genetic heterogeneityAmerican Journal of Medical Genetics, 1980