Talk:3q29 microdeletion syndrome

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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