Drupal-Biblio17<style face="normal" font="default" size="100%">MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutations of RUNX1 in families with inherited thrombocytopenia.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MYH9 gene mutations associated with bleeding.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MYH9-related disease: Report on five German families and description of a novel mutation.</style>