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.
Marker Type | Symbol | Name |
---|---|---|
Gene | fadd | Fas (tnfrsf6)-associated via death domain |
Gene | fgf3 | fibroblast growth factor 3 |