An example of parenchymal renal sparing in the context of complex malformations due to a novel mutation in the PBX1 gene

Author:

Ruscitti Federica1ORCID,Cerminara Maria12,Iascone Maria3,Pezzoli Laura3,Rosti Giulia12,Romano Ferruccio1,Ronchetto Patrizia4,Martucciello Giuseppe15,Buratti Silvia6,Buffelli Francesca7,Bocciardi Renata12,Puliti Aldamaria12,Divizia Maria Teresa2

Affiliation:

1. DINOGMI University of Genoa Genoa Italy

2. UOC Genetica Medica IRCCS Istituto Giannina Gaslini Genoa Italy

3. Laboratorio di Genetica Medica ASST Papa Giovanni XXIII Bergamo Italy

4. UOC Laboratorio di Genetica Umana IRCCS Istituto Giannina Gaslini Genoa Italy

5. UOC Chirurgia Pediatrica IRCCS Istituto Giannina Gaslini Genoa Italy

6. UOC Terapia Intensiva Neonatale e Pediatrica IRCCS Istituto Giannina Gaslini Genoa Italy

7. Fetal‐Perinatal Pathology Unit IRCCS Istituto Giannina Gaslini Genoa Italy

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Developmental Biology,Toxicology,Embryology,Pediatrics, Perinatology and Child Health

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