Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis, and interrupted aortic arch
Ibrahim, Masitah, Hunter, Matthew, Gugasyan, Lucy, Chan, Yuen, Malhotra, Atul, Sehgal, Arvind, Tan, KennethVolume:
5
Language:
english
Journal:
Clinical Case Reports
DOI:
10.1002/ccr3.759
Date:
February, 2017
File:
PDF, 1.84 MB
english, 2017