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Molecular Autism|November 5, 2011
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in malesRen-Hua Chung, Deqiong Ma, Kai Wang, et al.Plos One|October 22, 2011
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism riskDaria Salyakina, Holly N Cukier, Joycelyn M Lee, et al.BMC Medicine|October 23, 2009
Genomic and epigenetic evidence for oxytocin receptor deficiency in autismSimon G Gregory, Jessica J Connelly, Aaron J Towers, et al.Autism Research : Official Journal of the International Society for Autism Research|October 12, 2012
The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1Holly N Cukier, Joycelyn M Lee, Deqiong Ma, et al.American Journal of Medical Genetics|February 13, 2002
Genomic screen and follow-up analysis for autistic disorderYujun Shao, Chantelle M Wolpert, Kimberly L Raiford, et al.Human Molecular Genetics|May 1, 2012
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathwaysAnthony J Griswold, Deqiong Ma, Holly N Cukier, et al.Annals of Human Genetics|May 22, 2009
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1Deqiong Ma, Daria Salyakina, James M Jaworski, et al.Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.Pageof 3