1. De novo WNT5A‐associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. (24th May 2014) Authors: Roifman, M.; Marcelis, C.L.M.; Paton, T.; Marshall, C.; Silver, R.; Lohr, J.L.; Yntema, H.G.; Venselaar, H.; Kayserili, H.; van Bon, B.; Seaward, G.; FORGE Canada Consortium; Brunner, H.G.; Chitayat, D. Journal: Clinical genetics Issue: Volume 87:Number 1(2015:Jan.) Page Start: 34 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗