behavioral phenotype

Known as: behavioral phenotypes 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2017
0246819962017

Papers overview

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2016
2016
CD36 is a member of the class B scavenger receptor family of cell surface proteins, which plays a major role in fatty acid… (More)
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2015
2015
The maternal environment exerts important influences on offspring mass/growth, metabolism, reproduction, neurobiology, immune… (More)
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2015
2015
Cornelia de Lange syndrome (CdLS) is a congenital disorder characterized by distinctive facial features, growth retardation, limb… (More)
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2015
2015
In this study we describe the levels of clinically significant behavior in participants with Sotos syndrome relative to three… (More)
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2014
2014
Transactive response DNA-binding protein 43 (TDP-43) mislocalization and aggregation are hallmark features of amyotrophic lateral… (More)
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2014
2014
Fragile X syndrome (FXS) is a monogenic disease caused by mutations in the FMR1 gene. The Fmr1 knockout (KO) mice show many… (More)
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2014
2014
Evidence from clinical studies suggests that abnormal activity of brain derived neurotrophic factor (BDNF) contributes to the… (More)
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2013
2013
The 3q29 microdeletion syndrome is a rare, recurrent genomic disorder, associated with a variable phenotype, despite the same… (More)
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2003
2003
The clinical significance of an interstitial duplication of (15)(q11-q13) remains unclear and controversial. The reported… (More)
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1996
1996
Twenty 6- to 17-year-old children with neurofibromatosis 1. (NF1) were compared to 20 age- and sex-matched siblings on a wide… (More)
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