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Roos van der Donk

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European Journal of Human Genetics : EJHG|February 19, 2021
Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndromeAlexander J M Dingemans, Diante E Stremmelaar, Roos van der Donk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disordersRoos van der Donk, Sandra Jansen, Janneke H M Schuurs-Hoeijmakers, et al.
American Journal of Human Genetics|April 2, 2019
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial DysmorphismIllja J Diets, Roos van der Donk, Kristina Baltrunaite, et al.
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Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
European Journal of Human Genetics : EJHG|February 19, 2021
Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndromeAlexander J M Dingemans, Diante E Stremmelaar, Roos van der Donk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disordersRoos van der Donk, Sandra Jansen, Janneke H M Schuurs-Hoeijmakers, et al.
American Journal of Human Genetics|April 2, 2019
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial DysmorphismIllja J Diets, Roos van der Donk, Kristina Baltrunaite, et al.
Pageof 1