1-1 of 1
Keywords: FOXD1
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish

Subject Area:
Endocrinology , Further Areas , Genetics , Women's and Children's Health
I. Balikova, K. Devriendt, J.-P. Fryns, J.R. Vermeesch
Journal: Molecular Syndromology
Mol Syndromol (2011) 1 (5): 255–261.
https://doi.org/10.1159/000327707
Published Online: 18 May 2011
..., ANKRA2, FUNDC2P1, BTF3 and FOXD1 . The latter is expressed in the developing branchial arches and involved in cranio-facial development. Zebrafish embryos with combined inhibition of the expression of foxd1l and tfap2a show optic axis defects. We identified a novel locus associated with a mild BOFS-like...
View articletitled, FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish
Open the PDF for FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish in another window