Publication: Congenial heart disease revealing familial Velocardiofacial syndrome caused by 3 Mb deletion at 22q11 region
Loading...
Date
Advisor
Coadvisor
Graduate program
Undergraduate course
Journal Title
Journal ISSN
Volume Title
Publisher
Nature Publishing Group
Type
Abstract
Access right
Abstract
Description
Keywords
Language
English
Citation
European Journal Of Human Genetics. London: Nature Publishing Group, v. 26, p. 962-962, 2018.
