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Geraldine Van Winckel

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Molecular Genetics and Metabolism|April 7, 2023
Biotinidase deficiency: What have we learned in forty years?Aurel T Tankeu, Geraldine Van Winckel, Jolanda Elmers, et al.
Scientific Reports|January 11, 2024
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variantRoberto Ricciardiello, Giulia Forleo, Lina Cipolla, et al.
Molecular Genetics and Metabolism Reports|April 19, 2021
Classical homocystinuria, is it safe to exercise?Aurel T Tankeu, Geraldine Van Winckel, Belinda Campos-Xavier, et al.
Molecular Autism|October 27, 2021
De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizuresBeryl Royer-Bertrand, Marine Jequier Gygax, Katarina Cisarova, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Molecular Genetics and Metabolism|April 7, 2023
Biotinidase deficiency: What have we learned in forty years?Aurel T Tankeu, Geraldine Van Winckel, Jolanda Elmers, et al.
Scientific Reports|January 11, 2024
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variantRoberto Ricciardiello, Giulia Forleo, Lina Cipolla, et al.
Molecular Genetics and Metabolism Reports|April 19, 2021
Classical homocystinuria, is it safe to exercise?Aurel T Tankeu, Geraldine Van Winckel, Belinda Campos-Xavier, et al.
Molecular Autism|October 27, 2021
De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizuresBeryl Royer-Bertrand, Marine Jequier Gygax, Katarina Cisarova, et al.
Pageof 1