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Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features
Rami A. Ballout, Cheryl Dickerson, Myra J. Wick, Najla Al-Sweel, Amanda S. Openshaw, Siddharth Srivastava, Lindsay C. Swanson, Nuria C. Bramswig, Alma Kuechler, Bo Hong, Leah R. Fleming, Kathryn Curry, Stephen P. Robertson, Erica F. Andersen, Ayman W. El-Hattab
Research output: Contribution to journal › Article › peer-review
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