See integrated course of Pediatrics
Students are provided with knowledge about responsible genes and mechanisms of disease of monogenic hereditary diseases, including extensions due to genetic and allelic heterogeneity, penetrance and variable expression.
New diagnostic tools: CGH-Array and New Generation Sequencing.
Theoretical basis of complex hereditary diseases and the tools used to search genetic factors of susceptibility are discussed.
Recognize and classify the major congenital malformations, malformative syndromes and chromosomal illnesses
Identify environmental, external or intrauterine factors that may contribute to the handling of unfavorable hereditary characters and / or malformations
Traditional and molecular chromosome study
Approach to diseases with heterogeneous genetic etiology
Esome analysis
See integrated course of pediatrics
Ricevimento: Students must make an appointment to talk to professors. e-mail phone
ROBERTO CERONE (President)
MOHAMAD MAGHNIE (President)
CARLO BELLINI
RENATA BOCCIARDI
CLAUDIO BRUNO
PIER LUIGI BRUSCHETTINI
GIUSEPPE D'ANNUNZIO
ELISA DE GRANDIS
NATASCIA DI IORGI
ALBERTO FERRANDO
ROBERTO GASTALDI
GIAN MICHELE MAGNANO
MARIA MARGHERITA MANCARDI
GIUSEPPE MARTUCCIELLO
GIROLAMO MATTIOLI
ALBERTO MICHELAZZI
CARLO MINETTI
LAURA MINICUCCI
GUIDO MORCALDI
ALESSIO PINI PRATO
ALDAMARIA PULITI
LUCA ANTONIO RAMENGHI
ROBERTO RAVAZZOLO
ANGELO RAVELLI
OLIVIERO SACCO
MARGHERITA SAVOINI
MARIA CRISTINA SCHIAFFINO
PASQUALE STRIANO
MICHELE TORRE
EDVIGE MARIA VENESELLI
EUGENIO BONIOLI (President and Coordinator of Integrated Course)
see integrated cours of pediatrics
