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Showing results (691-700 of 719) with videos related to

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Nature Genetics|December 18, 2001
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiaSimon E Fisher, Clyde Francks, Angela J Marlow, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
Annals of Neurology|January 5, 2002
McLeod neuroacanthocytosis: genotype and phenotypeA Danek, J P Rubio, L Rampoldi, et al.
Genes, Brain, and Behavior|July 29, 2014
Genome-wide screening for DNA variants associated with reading and language traitsA Gialluisi, D F Newbury, E G Wilcutt, et al.
Human Mutation|September 18, 2010
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficitsDenise Horn, Johannes Kapeller, Núria Rivera-Brugués, et al.
Molecular Psychiatry|April 30, 2009
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibilityE Maestrini, A T Pagnamenta, J A Lamb, et al.
Genome Research|October 1, 1996
An integrated YAC map of the human X chromosomeH Roest Crollius, M T Ross, A Grigoriev, et al.
Nature Genetics|October 20, 2022
Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
Nature Genetics|February 24, 2023
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.
Pageof 72

Showing results (691-700 of 719) with videos related to

Sort By:
Pageof 72
Nature Genetics|December 18, 2001
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiaSimon E Fisher, Clyde Francks, Angela J Marlow, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
Annals of Neurology|January 5, 2002
McLeod neuroacanthocytosis: genotype and phenotypeA Danek, J P Rubio, L Rampoldi, et al.
Genes, Brain, and Behavior|July 29, 2014
Genome-wide screening for DNA variants associated with reading and language traitsA Gialluisi, D F Newbury, E G Wilcutt, et al.
Human Mutation|September 18, 2010
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficitsDenise Horn, Johannes Kapeller, Núria Rivera-Brugués, et al.
Molecular Psychiatry|April 30, 2009
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibilityE Maestrini, A T Pagnamenta, J A Lamb, et al.
Genome Research|October 1, 1996
An integrated YAC map of the human X chromosomeH Roest Crollius, M T Ross, A Grigoriev, et al.
Nature Genetics|October 20, 2022
Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
Nature Genetics|February 24, 2023
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
Biological Psychiatry|March 30, 2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexiaAlistair T Pagnamenta, Elena Bacchelli, Maretha V de Jonge, et al.
Pageof 72