1. FOXF2 is required for cochlear development in humans and mice. (17th December 2018) Authors: Bademci, Guney; Abad, Clemer; Incesulu, Armagan; Elian, Fahed; Reyahi, Azadeh; Diaz-Horta, Oscar; Cengiz, Filiz B; Sineni, Claire J; Seyhan, Serhat; Atli, Emine Ikbal; Basmak, Hikmet; Demir, Selma; Nik, Ali Moussavi; Footz, Tim; Guo, Shengru; Duman, Duygu; Fitoz, Suat; Gurkan, Hakan; Blanton, Sus... Journal: Human molecular genetics Issue: Volume 28:Number 8(2019) Page Start: 1286 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genomics and anterior segment dysgenesis: a review. (29th July 2013) Authors: Ito, Yoko A; Walter, Michael A Journal: Clinical & experimental ophthalmology Issue: Volume 42:Number 1(2014) Page Start: 13 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma. (17th December 2018) Authors: Lahola-Chomiak, Adrian A; Footz, Tim; Nguyen-Phuoc, Kim; Neil, Gavin J; Fan, Baojian; Allen, Keri F; Greenfield, David S; Parrish, Richard K; Linkroum, Kevin; Pasquale, Louis R; Leonhardt, Ralf M; Ritch, Robert; Javadiyan, Shari; Craig, Jamie E; Allison, W T; Lehmann, Ordan J; Walter, Michael A; ... Journal: Human molecular genetics Issue: Volume 28:Number 8(2019) Page Start: 1298 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗