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Association of candidate genes with phenotypic traits relevant to anorexia nervosa.
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
Perforin-dependent nuclear entry of granzyme B precedes apoptosis, and is not a consequence of nuclear membrane dysfunction.
Locomotor response to novelty predicts a rat's propensity to self-administer nicotine.
Linking the genetic architecture of cytosine modifications with human complex traits.
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Linking the genetic architecture of cytosine modifications with human complex traits.
Linking the genetic architecture of cytosine modifications with human complex traits. Hum Mol Genet. 2014 Nov 15; 23(22):5893-905.
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PubMed
subject areas
Cytosine
Genetics, Medical
Genome-Wide Association Study
Histones
Humans
Polymorphism, Single Nucleotide
Promoter Regions, Genetic
Quantitative Trait Loci
authors with profiles
Lucy Godley
Mary Dolan