Associated Papers
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM10_ESM.xlsx › Supplementary_Data_8
A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia.
Zhang H et al.
Bmc Medical Genetics, 2019
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