Talk:3q29 microdeletion syndrome

From Wikipedia, the free encyclopedia
Jump to: navigation, search
WikiProject Medicine (Rated Start-class, Low-importance)
WikiProject icon This article is within the scope of WikiProject Medicine, which recommends that medicine-related articles follow the Manual of Style for medicine-related articles and that biomedical information in any article use high-quality medical sources. Please visit the project page for details or ask questions at Wikipedia talk:WikiProject Medicine.
Start-Class article Start  This article has been rated as Start-Class on the project's quality scale.
 Low  This article has been rated as Low-importance on the project's importance scale.
 

Untitled[edit]

This article needs substantial revision. There are at least two case studies of children with normal cognitive function. This article doesn't begin to address the great variabilty in phenotype. Cgkleiber (talk) 18:44, 3 November 2011 (UTC)cgkleiber

William Cobb, Arne Anderson, Clesson Turner, Ruth D. Hoffman, Steven Schonberg, Sondra W. Levin, 1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child, European Journal of Medical Genetics, Volume 53, Issue 6, November-December 2010, Pages 415-418, ISSN 1769-7212, 10.1016/j.ejmg.2010.08.009. (http://www.sciencedirect.com/science/article/pii/S176972121000090X) Keywords: Deletion 3q29; IQ; Autism; Array CGH analysis

Feng Li, Emily C. Lisi, Elizabeth S. Wohler, Ada Hamosh, Denise A.S. Batista, 3q29 interstitial microdeletion syndrome: An inherited case associated with cardiac defect and normal cognition, European Journal of Medical Genetics, Volume 52, Issue 5, September-October 2009, Pages 349-352, ISSN 1769-7212, 10.1016/j.ejmg.2009.05.001. (http://www.sciencedirect.com/science/article/pii/S1769721209000597) Keywords: 3q29; Microdeletion; Microarray; PDA; Cardiac defect