Otofaciocervical syndrome: a sporadic patient supports splitting from the branchio-oto-renal syndrome

gan Dallapiccola, Bruno, Mingarelli, Rita
Cyhoeddwyd 1995

Abnormal skeletal phenotypes from simple signs to complex diagnoses /

gan Castriota-Scanderbeg, Alessandro., Dallapiccola, Bruno.
Cyhoeddwyd 2005

Acro-cardio-facial syndrome

gan Digilio, Maria Cristina, Dallapiccola, Bruno
Cyhoeddwyd 2010

Joubert Syndrome and related disorders

gan Brancati Francesco, Dallapiccola Bruno, Valente Enza
Cyhoeddwyd 2010-07-01

Orphanet Journal of Rare Diseases: Launch Editorial

gan Aymé, Ségolène, Dallapiccola, Bruno, Donnai, Dian
Cyhoeddwyd 2006

KBG syndrome

gan Brancati, Francesco, Sarkozy, Anna, Dallapiccola, Bruno
Cyhoeddwyd 2006

Potential of multiomics technology in precision medicine

gan Putignani, Lorenza, Gasbarrini, Antonio, Dallapiccola, Bruno
Cyhoeddwyd yn Curr Opin Gastroenterol (2019)

Leopard syndrome

gan Sarkozy, Anna, Digilio, Maria Cristina, Dallapiccola, Bruno
Cyhoeddwyd 2008

Joubert Syndrome and related disorders

gan Brancati, Francesco, Dallapiccola, Bruno, Valente, Enza Maria
Cyhoeddwyd 2010

Congenital heart defects in genetics syndromes

gan Digilio, M Cristina, Marino, Bruno, Dallapiccola, Bruno
Cyhoeddwyd yn Ital J Pediatr (2015)

Evidence for Interaction between Psoriasis-Susceptibility Loci on Chromosomes 6p21 and 1q21

gan Capon, Francesca, Semprini, Sabrina, Dallapiccola, Bruno, Novelli, Giuseppe
Cyhoeddwyd 1999

Clinical utility gene card for: Joubert syndrome

gan Valente, Enza Maria, Brancati, Francesco, Boltshauser, Eugen, Dallapiccola, Bruno
Cyhoeddwyd 2011

Clinical utility gene card for: Joubert Syndrome - update 2013

gan Valente, Enza Maria, Brancati, Francesco, Boltshauser, Eugen, Dallapiccola, Bruno
Cyhoeddwyd 2013

Mediterranean Diet and Health: Food Effects on Gut Microbiota and Disease Control

gan Del Chierico, Federica, Vernocchi, Pamela, Dallapiccola, Bruno, Putignani, Lorenza
Cyhoeddwyd 2014

Genetic prediction of common diseases. Still no help for the clinical diabetologist!

gan Prudente, Sabrina, Dallapiccola, Bruno, Pellegrini, Fabio, Doria, Alessandro, Trischitta, Vincenzo
Cyhoeddwyd 2012

In vivo Functional Genomics for Undiagnosed Patients: The Impact of Small GTPases Signaling Dysregulation at Pan-Embryo Developmental Scale

gan Lauri, Antonella, Fasano, Giulia, Venditti, Martina, Dallapiccola, Bruno, Tartaglia, Marco
Cyhoeddwyd yn Front Cell Dev Biol (2021)

Clinical utility gene card for: Mayer–Rokitansky–Küster–Hauser syndrome

gan Morcel, Karine, Dallapiccola, Bruno, Pasquier, Laurent, Watrin, Tanguy, Bernardini, Laura, Guerrier, Daniel
Cyhoeddwyd 2012

Survey of medical genetic services in Italy: year 2011

gan Giardino, Daniela, Mingarelli, Rita, Lauretti, Tiziana, Amoroso, Antonio, Larizza, Lidia, Dallapiccola, Bruno
Cyhoeddwyd yn BMC Health Serv Res (2016)

Identification of Type A, B, E, and F Botulinum Neurotoxin Genes and of Botulinum Neurotoxigenic Clostridia by Denaturing High-Performance Liquid Chromatography

gan Franciosa, Giovanna, Pourshaban, Manoocheher, De Luca, Alessandro, Buccino, Anna, Dallapiccola, Bruno, Aureli, Paolo
Cyhoeddwyd 2004

Connexin 26 variant carriers have a better gastrointestinal health: is this the heterozygote advantage?

gan Vuckovic, Dragana, Dallapiccola, Bruno, Franzè, Annamaria, Mauri, Lucia, Perrone, Maria Dolores, Gasparini, Paolo
Cyhoeddwyd yn Eur J Hum Genet (2015)