Sign in
  Edit search
Identification of ANKRD11 and ZNF778 as candidate genes for …
Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
Article, Chapter
Authors: M.H. Willemsen
Publication: European Journal of Human Genetics, Volume:18, Issue:4, Page(s):-435
Published: 2010
ISSN: 1018-4813
  Full text availability for this item
View Full Text Source:European Journal of Human Genetics,European Journal of Human Genetics,Springer Complete Journals Opens in new Window
Journal:  European Journal of Human Genetics Source:Springer Complete Journals Opens in new Window
Collection:  Springer Complete Journals Opens in new Window
Coverage:
  • 1993-01-01~present; volume:1~present;issue:1~present
View Full Text Source:European Journal of Human Genetics,European Journal of Human Genetics,PubMed Central Opens in new Window
Journal:  European Journal of Human Genetics Source:PubMed Central Opens in new Window
Collection:  PubMed Central Opens in new Window
Coverage:
  • 2009~12 months ago; volume:17~12 months ago
Browse related articles
  Print copies at your library
Check availability in RUQuest
  Request a copy of this item
Cite this item