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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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Dades bibliogràfiques
Publicat a:Neuroimage Clin
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5522376/
https://ncbi.nlm.nih.gov/pubmed/28761808
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2017.04.029
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