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Showing results (651-660 of 719) with videos related to

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Human Molecular Genetics|July 1, 1994
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.
Brain Structure & Function|August 12, 2016
Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout miceIsabel Martinez-Garay, Luiz G Guidi, Zoe G Holloway, et al.
Molecular Psychiatry|November 1, 2003
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII geneE Bacchelli, F Blasi, M Biondolillo, et al.
Molecular Psychiatry|November 20, 2003
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effectsS K Loo, S E Fisher, C Francks, et al.
American Journal of Human Genetics|May 7, 2005
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficitsKay D MacDermot, Elena Bonora, Nuala Sykes, et al.
Journal of Neurodevelopmental Disorders|January 18, 2014
Associations of HLA alleles with specific language impairmentRon Nudel, Nuala H Simpson, Gillian Baird, et al.
Plos One|November 10, 2010
Identification of candidate genes for dyslexia susceptibility on chromosome 18Thomas S Scerri, Silvia Paracchini, Andrew Morris, et al.
American Journal of Human Genetics|July 6, 2000
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorderC S Lai, S E Fisher, J A Hurst, et al.
The New England Journal of Medicine|November 7, 2008
A functional genetic link between distinct developmental language disordersSonja C Vernes, Dianne F Newbury, Brett S Abrahams, et al.
Genomics|April 11, 2000
Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemiaN McDonell, J Ramser, F Francis, et al.
Pageof 72

Showing results (651-660 of 719) with videos related to

Sort By:
Pageof 72
Human Molecular Genetics|July 1, 1994
X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletionsI Huber, M Bitner-Glindzicz, Y J de Kok, et al.
Brain Structure & Function|August 12, 2016
Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout miceIsabel Martinez-Garay, Luiz G Guidi, Zoe G Holloway, et al.
Molecular Psychiatry|November 1, 2003
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII geneE Bacchelli, F Blasi, M Biondolillo, et al.
Molecular Psychiatry|November 20, 2003
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effectsS K Loo, S E Fisher, C Francks, et al.
American Journal of Human Genetics|May 7, 2005
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficitsKay D MacDermot, Elena Bonora, Nuala Sykes, et al.
Journal of Neurodevelopmental Disorders|January 18, 2014
Associations of HLA alleles with specific language impairmentRon Nudel, Nuala H Simpson, Gillian Baird, et al.
Plos One|November 10, 2010
Identification of candidate genes for dyslexia susceptibility on chromosome 18Thomas S Scerri, Silvia Paracchini, Andrew Morris, et al.
American Journal of Human Genetics|July 6, 2000
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorderC S Lai, S E Fisher, J A Hurst, et al.
The New England Journal of Medicine|November 7, 2008
A functional genetic link between distinct developmental language disordersSonja C Vernes, Dianne F Newbury, Brett S Abrahams, et al.
Genomics|April 11, 2000
Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemiaN McDonell, J Ramser, F Francis, et al.
Pageof 72