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Showing results (671-680 of 719) with videos related to

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Genomics|February 16, 2000
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22A Bolino, E R Levy, M Muglia, et al.
Autism Research : Official Journal of the International Society for Autism Research|March 18, 2014
A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthmaFabiola Ceroni, Angela Sagar, Nuala H Simpson, et al.
Molecular Psychiatry|October 13, 2006
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexiaD Harold, S Paracchini, T Scerri, et al.
American Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.
American Journal of Human Genetics|August 21, 2002
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autismSusan L Smalley, Vlad Kustanovich, Sonia L Minassian, et al.
Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.
Elife|February 12, 2019
Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motilityWondwossen M Yeshaw, Marianne van der Zwaag, Francesco Pinto, et al.
Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.
Annals of Neurology|August 5, 2004
Chorein detection for the diagnosis of chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, Lea A Filippone, et al.
Translational Psychiatry|July 26, 2017
The DCDC2 deletion is not a risk factor for dyslexiaT S Scerri, E Macpherson, A Martinelli, et al.
Pageof 72

Showing results (671-680 of 719) with videos related to

Sort By:
Pageof 72
Genomics|February 16, 2000
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22A Bolino, E R Levy, M Muglia, et al.
Autism Research : Official Journal of the International Society for Autism Research|March 18, 2014
A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthmaFabiola Ceroni, Angela Sagar, Nuala H Simpson, et al.
Molecular Psychiatry|October 13, 2006
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexiaD Harold, S Paracchini, T Scerri, et al.
American Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.
American Journal of Human Genetics|August 21, 2002
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autismSusan L Smalley, Vlad Kustanovich, Sonia L Minassian, et al.
Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.
Elife|February 12, 2019
Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motilityWondwossen M Yeshaw, Marianne van der Zwaag, Francesco Pinto, et al.
Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.
Annals of Neurology|August 5, 2004
Chorein detection for the diagnosis of chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, Lea A Filippone, et al.
Translational Psychiatry|July 26, 2017
The DCDC2 deletion is not a risk factor for dyslexiaT S Scerri, E Macpherson, A Martinelli, et al.
Pageof 72