Showing results (21-30 of 28) with videos related to
Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Biological Psychiatry|April 1, 2008
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorderSusan L Christian, Camille W Brune, Jyotsna Sudi, et al.Plos One|February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genesRavinesh A Kumar, Christian R Marshall, Judith A Badner, et al.Brain : a Journal of Neurology|February 28, 2015
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasiaLaura A Jansen, Ghayda M Mirzaa, Gisele E Ishak, et al.European Journal of Human Genetics : EJHG|June 23, 2011
Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic functionAlex R Paciorkowski, Liu Lin Thio, Jill A Rosenfeld, et al.Plos Genetics|October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyriaSamin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.American Journal of Medical Genetics. Part A|June 7, 2008
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2William B Dobyns, Ghayda Mirzaa, Susan L Christian, et al.Nature Genetics|February 28, 2012
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndromeJean-Baptiste Rivière, Bregje W M van Bon, Alexander Hoischen, et al.Nature Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.Pageof 3