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European Journal of Human Genetics : EJHG
|
February 19, 2021
Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndrome
Alexander 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 disorders
Roos 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 Dysmorphism
Illja J Diets, Roos van der Donk, Kristina Baltrunaite, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 3) with videos related to
Sort By:
Page
of 1
European Journal of Human Genetics : EJHG
|
February 19, 2021
Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndrome
Alexander 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 disorders
Roos 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 Dysmorphism
Illja J Diets, Roos van der Donk, Kristina Baltrunaite, et al.
Page
of 1