Citations
Mayo Clinic
1 citation(s) found for "Curry, Kathryn".
Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features
Ballout, Rami A. , Dickerson, Cheryl, Wick, Myra , Al‐Sweel, Najla, Openshaw, Amanda, Srivastava, Siddharth , Swanson, Lindsay C., Bramswig, Nuria C. , Kuechler, Alma, Hong, Bo , Fleming, Leah , Curry, Kathryn, Andersen, Erica , El‐Hattab, Ayman W. , Wick, Myra J, El-Hattab, Ayman W , Robertson, Stephen P.
Human Mutation | February 29, 2020 | Volume: 41 | Issue: 7 | Pages: 1238-1249
