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Journal of Genetic Counseling|March 21, 2006
Parental perspectives on the causes of an autism spectrum disorder in their childrenL Mercer, S Creighton, J J A Holden, et al.Prenatal Diagnosis|March 26, 2005
Prenatally detected trisomy 20 mosaicismW P Robinson, B McGillivray, M E S Lewis, et al.Clinical Genetics|May 24, 2008
Autism-associated familial microdeletion of Xp11.22Y Qiao, X Liu, C Harvard, et al.Cytogenetic and Genome Research|March 17, 2009
Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disabilityY Qiao, C Harvard, N Riendeau, et al.Clinical Genetics|March 1, 2005
A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGHC Harvard, P Malenfant, M Koochek, et al.Human Genetics|June 1, 2010
Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformaticsY Qiao, C Harvard, C Tyson, et al.Journal of Medical Genetics|July 24, 2009
Phenomic determinants of genomic variation in autism spectrum disordersY Qiao, N Riendeau, M Koochek, et al.Clinical Genetics|January 26, 2006
15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGHM Koochek, C Harvard, M J Hildebrand, et al.Clinical Genetics|June 25, 2010
Autism severity is associated with child and maternal MAOA genotypesI L Cohen, X Liu, M E S Lewis, et al.Molecular Psychiatry|March 5, 2008
Face-brain asymmetry in autism spectrum disordersP Hammond, C Forster-Gibson, A E Chudley, et al.Pageof 2