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
Clinical and molecular consequences of disease-associated de novo mutations in SATB2.
Bengani H et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
Select a paper to view details