Jacqueline Chui

发表

Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGH

J. Weisfeld-Adams, J. Tepperberg, L. Mehta, 2011, American journal of medical genetics. Part A.

De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects

D. Schneidman-Duhovny, S. Dunwoodie, N. Pachter, 2017, Human molecular genetics.