Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations

Melanie MY Chan, Omid Sadeghi-Alavijeh, Seth du Preez, Catalin Voinescu, Loes van der Zanden, Sander Groen in 't Woud, Michiel Schreuder, Wout Feitz, Enrico Mingardo, Alina Hilger, Heiko Reutter, Lisanne Vendrig, Rik Westland, Glenda M Beaman, William Newman, Adrian S Woolf, Horia Stanescu, Adam Levine, Detlef Bockenhauer, Daniel P Gale
medRxiv 2024.10.10.24315242; doi:https://doi.org/10.1101/2024.10.10.24315242
Preprint
Jan 06, 2026
Consortium publication
No