Associated Papers
New insights into the phenotypic spectrum of 14q22q23 deletions: a case report and literature review.
Pichiecchio A et al.
Bmc Medical Genomics, 2018
Agnathia-otocephaly complex and asymmetric velopharyngeal insufficiency due to an in-frame duplication in OTX2.
Sergouniotis PI et al.
Journal of Human Genetics, 2015
The homeobox gene Otx2 in development and disease.
Beby F et al.
Experimental Eye Research, 2013
Recurrent agnathia-otocephaly caused by DNA replication slippage in PRRX1.
Dasouki M et al.
American Journal of Medical Genetics. Part A, 2013
OTX2 mutations contribute to the otocephaly-dysgnathia complex.
Chassaing N et al.
Journal of Medical Genetics, 2012
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