Clinical diagnostic exome sequencing identifies a maternally inherited 89 base pair deletion in the UBE3A gene associated with Angelman syndrome

Date:
Tuesday, Mar 24, 2015 12:00am – 12:00pm
Conference:
ACMG 2015
Authors:
Sha Tang, C. Michael Osborne, Christina L. Alamillo, Zöe Powis, Carrie Cain, Patricia G. Wheeler