Genitourinary Anomalies in Mowat-Wilson Syndrome with Deletion/Mutation in the Zinc Finger Homeo Box 1B Gene (ZFHX1B)
Livia Garavelli(Azienda Sanitaria Unità Locale di Reggio Emilia), Sergio Bernasconi(University of Parma), Marcella Zollino(Università Cattolica del Sacro Cuore), Guido Pastore(Università degli Studi del Piemonte Orientale “Amedeo Avogadro”), G Banchini, Simona Pedori(University of Parma), David Mowat(UNSW Sydney), Anita Rauch(University of Zurich), Michela Godi(Azienda Ospedaliera Sant'Andrea), P. Cerruti-Mainardi(Azienda Ospedaliera Sant'Andrea), S. Provera(Azienda Ospedaliera Sant'Andrea), R Virdis(University of Parma), Giovanni Neri(Catholic University of America), Nicola Longo(Center for Human Genetics), Christiane Zweier(University Hospital of Bern)
Cited by 18
Related Papers
Tuberous Sclerosis Complex Diagnostic Criteria Update: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
|Pediatric Neurology|2013|1.5k
Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
|Pediatric Neurology|2013|863
Treatment of Fabry’s Disease with the Pharmacologic Chaperone Migalastat
|New England Journal of Medicine|2016|555