Dickerson, Cheryl

Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features

Human Mutation | February 29, 2020 | Volume: 41 | Issue: 7 | Pages: 1238-1249

10.1002/humu.24009 | PMID 32112660