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Neurogenetics|June 14, 2006
Investigation of autism and GABA receptor subunit genes in multiple ethnic groupsAnn L Collins, Deqiong Ma, Patrice L Whitehead, et al.Neurogenetics|November 19, 2009
Novel variants identified in methyl-CpG-binding domain genes in autistic individualsHolly N Cukier, Raquel Rabionet, Ioanna Konidari, et al.Autism Research : Official Journal of the International Society for Autism Research|March 2, 2011
A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosisAnthony J Griswold, Deqiong Ma, Stephanie J Sacharow, et al.Neuroscience Letters|November 16, 2004
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genesRaquel Rabionet, James M Jaworski, Allison E Ashley-Koch, et al.American Journal of Human Genetics|March 5, 2002
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorderYujun Shao, Kimberly L Raiford, Chantelle M Wolpert, et al.American Journal of Medical Genetics|February 13, 2002
No association between the WNT2 gene and autistic disorderPinky A McCoy, Yujun Shao, Chantelle M Wolpert, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21Holly N Cukier, Daria Salyakina, Sarah F Blankstein, et al.Psychiatric Genetics|July 11, 2007
Investigation of potential gene-gene interactions between APOE and RELN contributing to autism riskAllison E Ashley-Koch, James Jaworski, De Qiong Ma, et al.The American Journal of Psychiatry|May 2, 2006
Lack of association between autism and SLC25A12Raquel Rabionet, Jacob L McCauley, James M Jaworski, et al.Annals of Human Genetics|November 8, 2012
Evaluating mitochondrial DNA variation in autism spectrum disordersAthena Hadjixenofontos, Michael A Schmidt, Patrice L Whitehead, et al.Pageof 3