1. Characterization of patients referred for non‐specific intellectual disability testing: the importance of autosomal genes for diagnosis. Issue 4 (15th March 2015) Authors: Tan, C.A.; Topper, S.; del Gaudio, D.; Nelakuditi, V.; Shchelochkov, O.; Nowaczyk, M.J.M.; Zeesman, S.; Brady, L.; Russell, L.; Meeks, N.; Sastry, S.; Arndt, K.; Kobiernicki, F.; Shaw, R.; Das, S. Journal: Clinical genetics Issue: Volume 89:Issue 4(2016) Page Start: 478 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?. (2nd April 2013) Authors: Nowaczyk, M.J.M.; Thompson, B.A.; Zeesman, S.; Moog, U.; Sanchez‐Lara, P.A.; Magoulas, P.L.; Falk, R.E.; Hoover‐Fong, J.E.; Batista, D.A.S.; Amudhavalli, S.M.; White, S.M.; Graham, G.E.; Rauen, K.A. Journal: Clinical genetics Issue: Volume 85:Number 2(2014:Feb.) Page Start: 138 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗