1. Delineation of clinical features in Wiedemann–Steiner syndrome caused by KMT2A mutations. Issue 1 (14th April 2015) Authors: Miyake, N.; Tsurusaki, Y.; Koshimizu, E.; Okamoto, N.; Kosho, T.; Brown, N.J.; Tan, T.Y.; Yap, P.J.J.; Suzumura, H.; Tanaka, T.; Nagai, T.; Nakashima, M.; Saitsu, H.; Niikawa, N.; Matsumoto, N. Journal: Clinical genetics Issue: Volume 89:Issue 1(2016) Page Start: 115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗