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Curry, Kathryn

St. Luke's Children's Genetics and Metabolic Clinic Boise Idaho

Citations 1

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