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Psychiatric Genetics
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August 20, 2004
Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders
Patrick F Bolton, Marijcke W M Veltman, Emma Weisblatt, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 28, 2018
Sex-chromosome dosage effects on gene expression in humans
Armin Raznahan, Neelroop N Parikshak, Vijay Chandran, et al.
European Journal of Human Genetics : EJHG
|
February 13, 2014
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment
Fabiola Ceroni, Nuala H Simpson, Clyde Francks, et al.
Developmental Medicine and Child Neurology
|
October 15, 2013
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
Nuala H Simpson, Laura Addis, William M Brandler, et al.
Plos Genetics
|
March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment
Pía Villanueva, Ron Nudel, Alexander Hoischen, et al.
American Journal of Human Genetics
|
January 3, 2012
Rare deletions at the neurexin 3 locus in autism spectrum disorder
Andrea K Vaags, Anath C Lionel, Daisuke Sato, et al.
Nature Reviews. Genetics
|
April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorder
Christian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
American Journal of Human Genetics
|
August 4, 2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairment
Dianne F Newbury, Laura Winchester, Laura Addis, et al.
European Journal of Human Genetics : EJHG
|
November 4, 2004
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q
Elena Bonora, Janine A Lamb, Gabrielle Barnby, et al.
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 66) with videos related to
Sort By:
Page
of 7
Psychiatric Genetics
|
August 20, 2004
Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders
Patrick F Bolton, Marijcke W M Veltman, Emma Weisblatt, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 28, 2018
Sex-chromosome dosage effects on gene expression in humans
Armin Raznahan, Neelroop N Parikshak, Vijay Chandran, et al.
European Journal of Human Genetics : EJHG
|
February 13, 2014
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment
Fabiola Ceroni, Nuala H Simpson, Clyde Francks, et al.
Developmental Medicine and Child Neurology
|
October 15, 2013
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
Nuala H Simpson, Laura Addis, William M Brandler, et al.
Plos Genetics
|
March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment
Pía Villanueva, Ron Nudel, Alexander Hoischen, et al.
American Journal of Human Genetics
|
January 3, 2012
Rare deletions at the neurexin 3 locus in autism spectrum disorder
Andrea K Vaags, Anath C Lionel, Daisuke Sato, et al.
Nature Reviews. Genetics
|
April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorder
Christian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
American Journal of Human Genetics
|
August 4, 2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairment
Dianne F Newbury, Laura Winchester, Laura Addis, et al.
European Journal of Human Genetics : EJHG
|
November 4, 2004
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q
Elena Bonora, Janine A Lamb, Gabrielle Barnby, et al.
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Page
of 7