Talk
Contribution of Whole-Genome Sequencing to Ocular Malformations: Review of One Hundred AURAGEN Cases
Contribution to an oral presentation at the 13th French Meeting of Human and Medical Genetics on whole-genome sequencing in ocular developmental anomalies.
Contribution to the oral presentation (submission #49269, session SS009) at the 13th French Meeting of Human and Medical Genetics, Cannes, January 2026, on the contribution of whole-genome sequencing to ocular malformations, based on one hundred cases sequenced within the AURAGEN program.