A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations
Bravo-Oro, Antonio, Lurie, Iosif W., Elizondo-Cárdenas, Gabriela, Peña-Zepeda, Claudia, Salazar-Martínez, Abel, Correa-González, Cecilia, Castrillo, José Luis, Avila, Silvia, Esmer, CarmenVolume:
167
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.36806
Date:
August, 2015
File:
PDF, 2.69 MB
english, 2015