Mohamed A. Youssef

RAX and anophthalmia in humans: Evidence of brain anomalies

P. Hauser, D. Schorderet, H. Abouzeid, 2012, Molecular vision.

Mutations in the SPARC-related modular calcium-binding protein 1 gene, SMOC1, cause waardenburg anophthalmia syndrome.

D. Schorderet, P. Descombes, F. Munier, 2011, American journal of human genetics.

PAX6 aniridia and interhemispheric brain anomalies

P. Hauser, D. Schorderet, F. Munier, 2009, Molecular vision.

Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia.

Ghada I. Gawdat, E. Marzouk, N. E. El Shakankiri, 2019, Advances in experimental medicine and biology.

Compound Heterozygous VSX2 Mutation Causing Bilateral Anophthalmia in a Consanguineous Egyptian Family

D. Schorderet, F. Munier, H. Abouzeid, 2015 .