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Human Genetics
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September 14, 2011
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia
Jose Felix Marti-Masso, Javier Ruiz-Martínez, Vladimir Makarov, et al.
BMC Medical Genetics
|
March 22, 2014
De novo SCN2A splice site mutation in a boy with Autism spectrum disorder
Teresa Tavassoli, Alexander Kolevzon, A Ting Wang, et al.
European Child & Adolescent Psychiatry
|
February 26, 2021
Systematic review and meta-analysis: relationships between attention-deficit/hyperactivity disorder and urinary symptoms in children
Behrang Mahjani, Lotta Renström Koskela, Christina Gustavsson Mahjani, et al.
Molecular Autism
|
July 3, 2015
Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
Neha Uppal, Rishi Puri, Frank Yuk, et al.
Brain and Behavior
|
August 17, 2021
Systematic review and meta-analysis identify significant relationships between clinical anxiety and lower urinary tract symptoms
Behrang Mahjani, Lotta Renström Koskela, Anita Batuure, et al.
Cell Reports
|
June 2, 2015
Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators
Lara J Duffney, Ping Zhong, Jing Wei, et al.
Biological Psychiatry
|
April 28, 2009
Gene expression patterns associated with posttraumatic stress disorder following exposure to the World Trade Center attacks
Rachel Yehuda, Guiqing Cai, Julia A Golier, et al.
Human Molecular Genetics
|
September 24, 2004
Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes
Nicholas J Bray, Luke Jehu, Valentina Moskvina, et al.
Brain, Behavior, and Immunity
|
May 24, 2018
Gene expression in cord blood links genetic risk for neurodevelopmental disorders with maternal psychological distress and adverse childhood outcomes
Michael S Breen, Aliza P Wingo, Nastassja Koen, et al.
Journal of Neurodevelopmental Disorders
|
April 24, 2021
FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring
Reymundo Lozano, Catherine Gbekie, Paige M Siper, et al.
Page
of 38
Search research articles
Search
Showing results (151-160 of 376) with videos related to
Sort By:
Page
of 38
Human Genetics
|
September 14, 2011
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia
Jose Felix Marti-Masso, Javier Ruiz-Martínez, Vladimir Makarov, et al.
BMC Medical Genetics
|
March 22, 2014
De novo SCN2A splice site mutation in a boy with Autism spectrum disorder
Teresa Tavassoli, Alexander Kolevzon, A Ting Wang, et al.
European Child & Adolescent Psychiatry
|
February 26, 2021
Systematic review and meta-analysis: relationships between attention-deficit/hyperactivity disorder and urinary symptoms in children
Behrang Mahjani, Lotta Renström Koskela, Christina Gustavsson Mahjani, et al.
Molecular Autism
|
July 3, 2015
Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
Neha Uppal, Rishi Puri, Frank Yuk, et al.
Brain and Behavior
|
August 17, 2021
Systematic review and meta-analysis identify significant relationships between clinical anxiety and lower urinary tract symptoms
Behrang Mahjani, Lotta Renström Koskela, Anita Batuure, et al.
Cell Reports
|
June 2, 2015
Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators
Lara J Duffney, Ping Zhong, Jing Wei, et al.
Biological Psychiatry
|
April 28, 2009
Gene expression patterns associated with posttraumatic stress disorder following exposure to the World Trade Center attacks
Rachel Yehuda, Guiqing Cai, Julia A Golier, et al.
Human Molecular Genetics
|
September 24, 2004
Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes
Nicholas J Bray, Luke Jehu, Valentina Moskvina, et al.
Brain, Behavior, and Immunity
|
May 24, 2018
Gene expression in cord blood links genetic risk for neurodevelopmental disorders with maternal psychological distress and adverse childhood outcomes
Michael S Breen, Aliza P Wingo, Nastassja Koen, et al.
Journal of Neurodevelopmental Disorders
|
April 24, 2021
FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring
Reymundo Lozano, Catherine Gbekie, Paige M Siper, et al.
Page
of 38