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Gina Conti-Ramsden

Showing results (81-90 of 88) with videos related to

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Journal of Neurodevelopmental Disorders|January 18, 2014
Associations of HLA alleles with specific language impairmentRon Nudel, Nuala H Simpson, Gillian Baird, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Genome-wide analysis identifies a role for common copy number variants in specific language impairmentNuala H Simpson, Fabiola Ceroni, Rose H Reader, et al.
European Journal of Human Genetics : EJHG|December 25, 2014
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'Fabiola Ceroni, Nuala H Simpson, Clyde Francks, et al.
European Journal of Human Genetics : EJHG|February 13, 2014
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairmentFabiola 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 dyslexiaNuala H Simpson, Laura Addis, William M Brandler, et al.
Plos Genetics|June 27, 2015
Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language ImpairmentPía Villanueva, Ron Nudel, Alexander Hoischen, et al.
Plos Genetics|March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairmentPía Villanueva, Ron Nudel, Alexander Hoischen, et al.
American Journal of Human Genetics|August 4, 2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairmentDianne F Newbury, Laura Winchester, Laura Addis, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Journal of Neurodevelopmental Disorders|January 18, 2014
Associations of HLA alleles with specific language impairmentRon Nudel, Nuala H Simpson, Gillian Baird, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Genome-wide analysis identifies a role for common copy number variants in specific language impairmentNuala H Simpson, Fabiola Ceroni, Rose H Reader, et al.
European Journal of Human Genetics : EJHG|December 25, 2014
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'Fabiola Ceroni, Nuala H Simpson, Clyde Francks, et al.
European Journal of Human Genetics : EJHG|February 13, 2014
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairmentFabiola 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 dyslexiaNuala H Simpson, Laura Addis, William M Brandler, et al.
Plos Genetics|June 27, 2015
Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language ImpairmentPía Villanueva, Ron Nudel, Alexander Hoischen, et al.
Plos Genetics|March 18, 2015
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairmentPía Villanueva, Ron Nudel, Alexander Hoischen, et al.
American Journal of Human Genetics|August 4, 2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairmentDianne F Newbury, Laura Winchester, Laura Addis, et al.
Pageof 9