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  3. Whole-genome Sequencing Reveals Contribution of Rare and Common Variation To Structural Kidney and Urinary Tract Malformations

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

Chan MMY, Sadeghi-Alavijeh O, Voinescu CD, van der Zanden LFM, Woud SG, Schreuder MF, Feitz W, Mingardo E, Hilger AC, Reutter H, Vendrig LM, Westland R, Stanescu HC, Levine AP, Böckenhauer D, Gale DP.
medRxiv 2024.10.10.24315242; doi: https://doi.org/10.1101/2024.10.10.24315242
https://www.medrxiv.org/content/10.1101/2024.10.10.24315242v1
Preprint
Oct 10, 2024

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The University of Helsinki is the organization responsible for the FinnGen research project. The Finnish consortium partners include all Finnish public biobanks and their background organisations, so the project covers the whole of Finland. All partners are listed on this page.

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