Genetics of kidney disorders in Phelan-McDermid syndrome: evidence from 357 registry participants
Article in Pediatric Nephrology (September 2023)
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Whole exome sequencing identifies KIF26B, LIFR and LAMC1 mutations in familial vesicoureteral reflux
Article in PLOS ONE (November 2022)
Anomalías congénitas del riñón y las vías urinarias
Article in EMC - Pediatría (August 2022)