Expanding the phenotype of ASXL3-related syndrome: a comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3. Am J Med Genet A. 2021;185A(11):3446-3458. Doi:10.1002/ajmg.a.62465″

Am J Med Genet A. 2023 Jan;191(1):310. doi: 10.1002/ajmg.a.62993. Epub 2022 Oct 12.
No abstract available

Publication types

  • Published Erratum