Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders

PURPOSE: The interpretation of genetic variants after genome-wide analysis is complex in heterogeneous disorders such as intellectual disability (ID). We investigate whether algorithms can be used to detect if a facial gestalt is present for three novel ID syndromes and if these techniques can help...

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Detalles Bibliográficos
Autores principales: van der Donk, Roos, Jansen, Sandra, Schuurs-Hoeijmakers, Janneke H. M., Koolen, David A., Goltstein, Lia C. M. J., Hoischen, Alexander, Brunner, Han G., Kemmeren, Patrick, Nellåker, Christoffer, Vissers, Lisenka E. L. M., de Vries, Bert B. A., Hehir-Kwa, Jayne Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752476/
https://www.ncbi.nlm.nih.gov/pubmed/30568311
http://dx.doi.org/10.1038/s41436-018-0404-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752476/
https://www.ncbi.nlm.nih.gov/pubmed/30568311
http://dx.doi.org/10.1038/s41436-018-0404-y

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