Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)
- 13 August 2008
- journal article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 17 (1) , 14-21
- https://doi.org/10.1038/ejhg.2008.141
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- FGF8 initiates inner ear induction in chick and mouseGenes & Development, 2005
- Molecular characteristics of fibroblast growth factor–fibroblast growth factor receptor–heparin-like glycosaminoglycan complexProceedings of the National Academy of Sciences, 1999
- Structure and expression of a novel human FGF, FGF-19, expressed in the fetal brainBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1999
- PedCheck: A Program for Identification of Genotype Incompatibilities in Linkage AnalysisAmerican Journal of Human Genetics, 1998
- Fibroblast Growth Factor 3, a Protein with Dual Subcellular Localization, Is Targeted to the Nucleus and Nucleolus by the Concerted Action of Two Nuclear Localization Signals and a Nucleolar Retention SignalPublished by Elsevier ,1997
- Refinement of the structure of human basic fibroblast growth factor at 1.6 Å resolution and analysis of presumed heparin binding sites by selenate substitutionProtein Science, 1993
- The int-2 proto-oncogene is responsible for induction of the inner earNature, 1991
- Genetic Epidemiology of Hearing ImpairmentAnnals of the New York Academy of Sciences, 1991
- Three-dimensional structure of human basic fibroblast growth factor, a structural homolog of interleukin 1 beta.Proceedings of the National Academy of Sciences, 1991
- Three-Dimensional Structures of Acidic and Basic Fibroblast Growth FactorsScience, 1991