Drupal-Biblio17<style face="normal" font="default" size="100%">Puzzling Results from Germline Mutations Analysis in a Group of Asbestos-Exposed Patients in a High-risk Area of Northeast Italy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Abnormal expression of leiomyoma cytoskeletal proteins involved in cell migration.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Autosomal recessive Stickler syndrome due to a loss of function mutation in the COL9A3 gene.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Next generation sequencing in nonsyndromic intellectual disability: from a negative molecular karyotype to a possible causative mutation detection.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The p53 transcriptional pathway is preserved in ATMmutated and NOTCH1mutated chronic lymphocytic leukemias.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">TNF-α SNP rs1800629 and risk of relapse in childhood acute lymphoblastic leukemia: relation to immunophenotype.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian family.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetics of food preferences: a first view from silk road populations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">High-throughput genotyping robot-assisted method for mutation detection in patients with hypertrophic cardiomyopathy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Vertebral defects in patients with Peters plus syndrome and mutations in B3GALTL.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A 3'UTR SNP in NLRP3 gene is associated with susceptibility to HIV-1 infection.</style>