Molecular, clinical and neuropsychological study in 31 patients with Kabuki syndrome and KMT2D mutations
Lehman, N., Mazery, A.C., Visier, A., Baumann, C., Lachesnais, D., Capri, Y., Toutain, A., Odent, S., Mikaty, M., Goizet, C., Taupiac, E., Jacquemont, M.L., Sanchez, E., Schaefer, E., Gatinois, V., FaJournal:
Clinical Genetics
DOI:
10.1111/cge.13010
Date:
May, 2017
File:
PDF, 1.17 MB
2017
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