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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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Bibliografski detalji
Izdano u:Neuroimage Clin
Glavni autori: 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
Jezik:Inglês
Izdano: Elsevier 2017
Teme:
Online pristup: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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