Publications

Export 2 results:
Author Title [ Year(Asc)]
Filters: First Letter Of Last Name is C and Author is Cheng, Hanyin  [Clear All Filters]
2019
Liu, P. et al. Reanalysis of Clinical Exome Sequencing Data. N Engl J Med 380, 2478-2480 (2019).
2018
Cheng, H. et al. Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies. Am J Hum Genet 102, 985-994 (2018).