We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleOTX2 microphthalmia syndrome: four novel mutations and delineation of a phenotypeAuthorsSchilter, KF; Schneider, A; Bardakjian, T; Soucy, J-F; Tyler, RC; Reis, LM; Semina, EVPublicationClinical Genetics, 2011, Vol 79, Issue 2, p158ISSN0009-9163Publication typearticleDOI10.1111/j.1399-0004.2010.01450.x