Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the Connexin 43 gene
- 30 September 2007
- journal article
- case report
- Published by Elsevier BV in International Journal of Oral & Maxillofacial Surgery
- Vol. 36 (9), 858-860
- https://doi.org/10.1016/j.ijom.2007.03.004
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Co-expression and regulation of connexins 36 and 43 in cultured neonatal rat pancreatic isletsCanadian Journal of Physiology and Pharmacology, 2005
- A novel GJA1 mutation causes oculodentodigital dysplasia without syndactylyAmerican Journal of Medical Genetics Part A, 2005
- Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital DysplasiaAmerican Journal of Human Genetics, 2003
- Gap junction proteins exhibit early and specific expression during intramembranous bone formation in the developing chick mandibleBrain Structure and Function, 1994
- Oculodentodigital syndrome: report of a case.Dentomaxillofacial Radiology, 1991
- Malocclusion and orthodontic treatment need of 15–74‐year‐old Dutch adultsCommunity Dentistry and Oral Epidemiology, 1991
- Oculodentodigital dysplasiaThe Journal of Pediatrics, 1963