Drupal-Biblio17<style face="normal" font="default" size="100%">Genotypic characterization and antimicrobial susceptibility of human isolates in Southern Spain.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes.</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%">Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient.</style>