Chassaing et al., 2012
- OTX2 mutations contribute to the otocephaly-dysgnathia complex.
Journal of Medical Genetics
49(6):373-379
Full text @ J. Med. Genet.
Target | Reagent |
---|---|
msx1a | MO2-msx1a |
otx2b | MO3-otx2b |
pgap1 | MO1-pgap1 |
prrx1a | MO1-prrx1a |
prrx1b | MO1-prrx1b |