Investigation of the GSα gene in the diagnosis of fibrous dysplasia
- 1 July 2004
- journal article
- case report
- Published by Elsevier in International Journal of Oral & Maxillofacial Surgery
- Vol. 33 (5) , 498-501
- https://doi.org/10.1016/j.ijom.2003.10.016
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Gsα gene mutations in monostotic fibrous dysplasia of bone and fibrous dysplasia-like low-grade central osteosarcomaVirchows Archiv, 2001
- Benign Fibro-Osseous Lesions: A Review of Current ConceptsAdvances in Anatomic Pathology, 2001
- Craniofacial fibrous dysplasia of the fronto-orbital region: A case series and literature reviewJournal of Oral and Maxillofacial Surgery, 2001
- A Comparative Study of Fibrous Dysplasia and Osteofibrous Dysplasia with Regard to GSα Mutation at the Arg201 CodonThe Journal of Molecular Diagnostics, 2000
- Etiology of fibrous dysplasia and McCune-Albright syndromeInternational Journal of Oral & Maxillofacial Surgery, 1999
- Cranio‐facial fibrous dysplasia in a 38‐year‐old African woman: a case historyOral Diseases, 1999
- Reproduction of human fibrous dysplasia of bone in immunocompromised mice by transplanted mosaics of normal and Gsalpha-mutated skeletal progenitor cells.Journal of Clinical Investigation, 1998
- Polymerase chain reaction-based technique for the selective enrichment and analysis of mosaic arg201 mutations in Gαs from patients with fibrous dysplasia of boneBone, 1997
- Polyostotic fibrous dysplasia: An unusual presentation in childhoodJournal of Oral and Maxillofacial Surgery, 1996