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An Example of Parenchymal Renal Sparing in the Context of Complex Malformations Due to a Novel Mutation in the PBX1 Gene

Federica Ruscitti,Maria Cerminara,Maria Iascone,Laura Pezzoli,Giulia Rosti,Ferruccio Romano,Patrizia Ronchetto,Giuseppe Martucciello,Silvia Buratti,Francesca Buffelli,Renata Bocciardi,Aldamaria Puliti,Maria Teresa Divizia

Birth defects research（2022）

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CAKUT,development,homeodomain,kidney,PBX1,WES
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