Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development
- 1 November 2007
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 81 (5), 906-912
- https://doi.org/10.1086/522240
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Dentin Matrix Protein 4, a Novel Secretory Calcium-binding Protein That Modulates Odontoblast DifferentiationPublished by Elsevier BV ,2007
- Raine syndrome: report of a family with three affected sibs and further delineation of the syndromeClinical Dysmorphology, 2003
- Multiple sequence alignment with the Clustal series of programsNucleic Acids Research, 2003
- Further delineation of Raine syndromeClinical Dysmorphology, 2003
- Raine dysplasia: a Brazilian case with a mild radiological involvementClinical Dysmorphology, 2000
- Intracranial calcification in Raine syndromePediatric Radiology, 1996
- Osteopetrosis: Brain ultrasound and computed tomography findingsEuropean Journal of Pediatrics, 1992
- New distinct lethal osteosclerotic bone dysplasia (Raine syndrome)American Journal of Medical Genetics, 1992
- A new lethal sclerosing bone dysplasiaSkeletal Radiology, 1991
- Unknown syndrome: microcephaly, hypoplastic nose, exophthalmos, gum hyperplasia, cleft palate, low set ears, and osteosclerosis.Journal of Medical Genetics, 1989