Amber de Haan
3PUBLICATIONS
4CO-AUTHORS
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Publications (3)
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|Nov 19, 2024
Genetic testing in a national cohort of adults with chronic kidney disease of unknown origin.Amber de Haan, Mark Eijgelsheim, Liffert Vogt
|Apr 03, 2023
Fabry disease with atypical phenotype identified by massively parallel sequencing in early-onset kidney failure.Amber de Haan, Chantal F Morel, Mark Eijgelsheim
|Apr 08, 2022
Diagnostic yield of massively parallel sequencing in patients with chronic kidney disease of unknown etiology: rationale and design of a national prospective cohort study.Amber de Haan, Mark Eijgelsheim, Liffert Vogt
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