1. Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophies. Issue 2 (22nd December 2017) Authors: Kakar, Naseebullah; Horn, Denise; Decker, Eva; Sowada, Nadine; Kubisch, Christian; Ahmad, Jamil; Borck, Guntram; Bergmann, Carsten Journal: American journal of medical genetics Issue: Volume 176:Issue 2(2018) Page Start: 438 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗