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Keywords: Branchio-oculo-facial syndrome
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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
...I. Balikova; K. Devriendt; J.-P. Fryns; J.R. Vermeesch Branchio-oculo-facial syndrome (BOFS) is a rare disorder characterized by maldevelopment of the first and second branchial arches, skin defects, facial dysmorphism, auricular, ophthalmological and oral abnormalities. A high clinical variability...
View article titled, FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the <span class="search-highlight">Branchio</span>-<span class="search-highlight">Oculo</span>-<span class="search-highlight">Facial</span> <span class="search-highlight">Syndrome</span> in Causing Eye Effects in Zebrafish
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