Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study

Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a genetic neurodevelopmental syndrome that has been studied intensively in order to understand relationships between the genetic microdeletion, brain development, cognitive function, and the emergence of psychiatric symptoms. White matter microstru...

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Detalles Bibliográficos
Autores principales: Tylee, Daniel S., Kikinis, Zora, Quinn, Thomas P., Antshel, Kevin M., Fremont, Wanda, Tahir, Muhammad A., Zhu, Anni, Gong, Xue, Glatt, Stephen J., Coman, Ioana L., Shenton, Martha E., Kates, Wendy R., Makris, Nikos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522376/
https://www.ncbi.nlm.nih.gov/pubmed/28761808
http://dx.doi.org/10.1016/j.nicl.2017.04.029

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522376/
https://www.ncbi.nlm.nih.gov/pubmed/28761808
http://dx.doi.org/10.1016/j.nicl.2017.04.029

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