Bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features: A newly recognized type of osteogenesis imperfecta
- 1 January 1987
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 110 (1), 76-80
- https://doi.org/10.1016/s0022-3476(87)80292-5
Abstract
No abstract availableFunding Information
- National Institutes of Health
This publication has 6 references indexed in Scilit:
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- Heritable Diseases of CollagenNew England Journal of Medicine, 1984
- Invited editorial comment: Osteogenesis imperfecta: Update and perspectiveAmerican Journal of Medical Genetics, 1984
- The syndrome of multisynostotic osteodysgenesis with long-bone fracturesAmerican Journal of Medical Genetics, 1980
- Genetic heterogeneity in osteogenesis imperfecta.Journal of Medical Genetics, 1979
- Eye Signs of HypophosphatasiaArchives of Ophthalmology (1950), 1969