Periventricular nodular heterotopia and bilateral intraventricular xanthogranulomas in 22q11.2 deletion syndrome

22q11.2 deletion syndrome (22q11DS) is the most common pathogenic copy number variant in humans. Neuropsychiatric phenotypes, including schizophrenia, are prominent. Imaging studies of individuals with this syndrome show a variety of abnormalities that may indicate abnormal neuronal migration. Here...

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Bibliographic Details
Main Authors: Moogeh Baharnoori (Author), Daniel M. Mandell (Author), Danielle M. Andrade (Author), Eva W.C. Chow (Author), Anne S. Bassett (Author), Tim-Rasmus Kiehl (Author)
Format: Book
Published: Elsevier, 2017-09-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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