Incidental Radiologic Findings in the 22q11.2 Deletion Syndrome

BACKGROUND AND PURPOSE: The 22q11.2 deletion syndrome is a common genetic microdeletion syndrome that results in cognitive delays and an increased risk of several psychiatric disorders, particularly schizophrenia. The current study investigates the prevalence of incidental neuroradiologic findings w...

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Detalles Bibliográficos
Publicado en:AJNR Am J Neuroradiol
Autores principales: Schmitt, J.E., Yi, J.J., Roalf, D.R., Loevner, L.A., Ruparel, K., Whinna, D., Souders, M.C., McDonald-McGinn, D.M., Yodh, E., Vandekar, S., Zackai, E.H., Gur, R.C., Emanuel, B.S., Gur, R.E.
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society of Neuroradiology 2014
Materias:
Pediatrics
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4440788/
https://ncbi.nlm.nih.gov/pubmed/24948496
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A4003
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