Clinical diagnostic exome sequencing identifies a maternally inherited 89
base pair deletion in the UBE3A gene associated with Angelman syndrome
Title: Clinical diagnostic exome sequencing identifies a maternally inherited 89
base pair deletion in the UBE3A gene associated with Angelman syndrome
Authors: C. Michael Osborne; Christina L. Alamillo; Zöe Powis; Carrie Cain; Patricia G. Wheeler; Sha Tang