Drupal-Biblio17<style face="normal" font="default" size="100%">The Mutational Landscape of Acute Promyelocytic Leukemia Reveals an Interacting Network of Co-Occurrences and Recurrent Mutations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Using activation status of signaling pathways as mechanism-based biomarkers to predict drug sensitivity.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Exome sequencing identifies a new mutation in SERAC1 in a patient with 3-methylglutaconic aciduria.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Discovering the hidden sub-network component in a ranked list of genes or proteins derived from genomic experiments.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient.</style>