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:
C. Michael Osborne, Carrie Cain, Christina L. Alamillo, Patricia G. Wheeler, Sha Tang, Zöe Powis