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Clinical Genetics|July 26, 2024
Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorderYoeri Sleyp, Harold S Matthews, Michiel Vanneste, et al.Journal of Medical Genetics|November 20, 2025
Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndromeMichiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.Medrxiv : the Preprint Server for Health Sciences|June 10, 2025
Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat SyndromeMichiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.Nature Genetics|April 6, 2021
Shared heritability of human face and brain shapeSahin Naqvi, Yoeri Sleyp, Hanne Hoskens, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 10, 2022
De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorderYoeri Sleyp, Irene Valenzuela, Andrea Accogli, et al.Nature Communications|October 2, 2020
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disordersTianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.Nature Communications|October 22, 2020
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disordersTianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.Pageof 1