Expanding the phenotype of <scp><i>ASXL3</i></scp>‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in <scp><i>ASXL3</i></scp>Schaida Schirwani, Charlotte W. Ockeloen, Julie Vogt et al.|American Journal of Medical Genetics Part A|2021Cited by 25