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behavioral phenotype

Known as: behavioral phenotypes 
 
National Institutes of Health

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… Expand
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2016
2016
This study was undertaken to describe seizure phenotypes, natural progression, sleep-wake patterns, as well as periodicity of… Expand
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Highly Cited
2015
Highly Cited
2015
The maternal environment exerts important influences on offspring mass/growth, metabolism, reproduction, neurobiology, immune… Expand
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2015
2015
Cornelia de Lange syndrome (CdLS) is a congenital disorder characterized by distinctive facial features, growth retardation, limb… Expand
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2015
2015
BACKGROUND We hypothesized intrauterine growth restricted offspring (IUGR) demonstrate higher rates of aggression and higher… Expand
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Highly Cited
2014
Highly Cited
2014
Fragile X syndrome (FXS) is a monogenic disease caused by mutations in the FMR1 gene. The Fmr1 knockout (KO) mice show many… Expand
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2014
2014
Transactive response DNA-binding protein 43 (TDP-43) mislocalization and aggregation are hallmark features of amyotrophic lateral… Expand
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2014
2014
Cornelia de Lange syndrome (CdLS) is a cohesinopathy causing delayed growth and limb deficits. Individuals with CdLS have mild to… Expand
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2013
2013
Behavioral, physiological, and life-history traits can be modified through interactions with environmental conditions during… Expand
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2013
2013
The 3q29 microdeletion syndrome is a rare, recurrent genomic disorder, associated with a variable phenotype, despite the same… Expand
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