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Title

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

CollaborationWith : Eliez, Stéphan / Schneider, Maude
Published in American Journal of Psychiatry. 2017, p. appiajp201716121417
Abstract Chromosome 22q11.2 deletion syndrome (22q11.2DS) is associated with a more than 20-fold increased risk for developing schizophrenia. The aim of this study was to identify additional genetic factors (i.e., "second hits") that may contribute to schizophrenia expression.
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PMID: 28750581
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Article (Published version) (567 Kb) - document accessible for UNIGE members only Limited access to UNIGE
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Research group Laboratoire d'imagerie et de psychopathologie développementale (693)
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(ISO format)
INTERNATIONAL CHROMOSOME 22Q11.2 CONSORTIUM, BRAIN AND BEHAVIOR CONSORTIUM. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome. In: American Journal of Psychiatry, 2017, p. appiajp201716121417. https://archive-ouverte.unige.ch/unige:97041

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Deposited on : 2017-09-26

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