Identification of a genetic cause for isolated unilateral coronal synostosis: A unique mutation in the fibroblast growth factor receptor 3
- 1 April 1998
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 132 (4) , 714-716
- https://doi.org/10.1016/s0022-3476(98)70366-x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosisThe Lancet, 1997
- Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromesNature Genetics, 1996
- A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiaNature Genetics, 1995
- Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3Nature Genetics, 1995
- Genetic study of nonsyndromic coronal craniosynostosisAmerican Journal of Medical Genetics, 1995
- Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasiaNature, 1994
- Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasiaPublished by Elsevier ,1994
- Assocition between “plagiocephaly” and hemifacial microsomiaAmerican Journal of Medical Genetics, 1993
- Frontal Plagiocephaly: Synostotic, Compensational, or DeformationalPlastic and Reconstructive Surgery, 1992
- Intrauterine Constraint and CraniosynostosisNeurosurgery, 1980