Wiedemann-Steiner Syndrome With 2 Novel <i>KMT2A</i> MutationsJung Min Ko, Tae‐Joon Cho, Yongjin Yoo et al.|Journal of Child Neurology|2016Cited by 27
Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred populationYoungha Lee, Jong‐Hee Chae, Murim Choi et al.|Scientific Reports|2020Cited by 5