Showing results (1-10 of 121) with videos related to
Sort By:
Pageof 13
Molecular Cytogenetics|August 16, 2014
A new patient with a terminal de novo 2p25.3 deletion of 1.9 Mb associated with early-onset of obesity, intellectual disabilities and hyperkinetic disorderMaria Clara Bonaglia, Roberto Giorda, Sergio ZaniniEuropean Journal of Human Genetics : EJHG|October 18, 2012
Low-copy repeats at the human VIPR2 gene predispose to recurrent and nonrecurrent rearrangementsSilvana Beri, Maria Clara Bonaglia, Roberto GiordaBrain & Development|September 4, 2019
Mild epileptic phenotype associates with de novo eef1a2 mutation: Case report and reviewMarta De Rinaldis, Roberto Giorda, Antonio TrabaccaDevelopmental Cognitive Neuroscience|June 12, 2012
Influence of the OPRM1 gene polymorphism upon children's degree of withdrawal and brain activation in response to facial expressionsEleonora Bertoletti, Annalisa Zanoni, Roberto Giorda, et al.Neuroscience and Biobehavioral Reviews|November 7, 2016
SLC6A4 methylation as an epigenetic marker of life adversity exposures in humans: A systematic review of literatureLivio Provenzi, Roberto Giorda, Silvana Beri, et al.American Journal of Medical Genetics. Part A|December 8, 2005
A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: cytogenetics, molecular, and methylation studiesGiorgio Gimelli, Roberto Giorda, Silvana Beri, et al.Frontiers in Endocrinology|November 23, 2017
Telomere Length in Preterm Infants: A Promising Biomarker of Early Adversity and Care in the Neonatal Intensive Care Unit?Livio Provenzi, Giunia Scotto di Minico, Roberto Giorda, et al.European Child & Adolescent Psychiatry|July 12, 2014
The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problemsValentina Riva, Cecilia Marino, Roberto Giorda, et al.Epilepsia Open|April 24, 2024
A de novo pathogenic variant in MICAL-1 causes epilepsy with auditory featuresPaolo Bonanni, Roberto Giorda, Roberto Michelucci, et al.Molecular Cytogenetics|November 20, 2015
Long-term follow-up of a patient with 5q31.3 microdeletion syndrome and the smallest de novo 5q31.2q31.3 deletion involving PURAMaria Clara Bonaglia, Nicoletta Zanotta, Roberto Giorda, et al.Pageof 13