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TypeTitleAuthor(s)YearViews
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5CGrafodatskaya, D; Chung, BHY; Butcher, DJ; Turinsky, AL; Goodman, SJ; Choufani, S; Chen, YA; Lou, Y; Zhao, C; Rajendram, R; Abidi, FE; Skinner, C; Stavropoulos, J; Bondy, CA; Hamilton, J; Wodak, S; Scherer, SW; Schwartz, CE; Weksberg, R201343
 
Crosstalk between histone modification and DNA methylation in patients with intellectual disability syndrome due to JARID1C mutationsChung, BHY; Grafodatskaya, D; Butcher, DT; Scherer, SW; Abidi, FE; Schwartz, CE; Wekserg, R2011107
 
Role of epigenetic dysregulation in neurodevelopmental syndromes: lessons from KDM5C mutationsGrafodatskaya, D; Chung, BHY; Butcher, DT; Goodman, S; Choufan, S; Lou, Y; Zhao, C; Rajendram, R; Abidi, FE; Skinner, C; Hamilton, J; Scherer, SW; Schwartz, CE; Weksberg, R2011112
 
Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutationsChung, BHY; Grafodatskaya, D; Butcher, DT; Scherer, SW; Abidi, FE; Schwartz, CE; Weksberg, R201087
 
Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutationsChung, B; Grafodatskaya, D; Butcher, DT; Scherer, SW; Abidi, FE; Schwartz, CE; Weksberg, R2010159
 
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