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.
5 Genes / Markers
Marker Type Symbol Name
Gene msx1a muscle segment homeobox 1a
Gene otx2b orthodenticle homeobox 2b
Gene pgap1 post-GPI attachment to proteins inositol deacylase 1
Gene prrx1a paired related homeobox 1a
Gene prrx1b paired related homeobox 1b
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