Gregory-Evans et al., 2007 - SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma. Human molecular genetics   16(20):2482-2493 Full text @ Hum. Mol. Genet.
2 Genes / Markers
Marker Type Symbol Name
Gene fadd Fas (tnfrsf6)-associated via death domain
Gene fgf3 fibroblast growth factor 3