Abouzeid, HanaYoussef, Mohamed A.Bayoumi, NaderElShakankiri, NihalMarzouk, ImanHauser, PhilippeSchorderet, Daniel F.2012-06-292012-06-292012-06-292012https://infoscience.epfl.ch/handle/20.500.14299/82459WOS:000304981700002Purpose: To report the clinical and genetic study of two families of Egyptian origin with clinical anophthalmia. To further determine the role of the retina and anterior neural fold homeobox gene (RAX) in anophthalmia and associated cerebral malformations.Vertebrate Eye DevelopmentHomeobox GeneColoboma MacMicrophthalmiaMutationsRxtext::journal::journal article::research article