An analysis of 21,094 patients with schizophrenia and 20,227 control individuals found 8 CNVs with a highly significant association (odds ratio of 0.15 to 67.7), with deletions 1q21.1, 2p16.3, 3q29, 15q13.3, 16p11.2, and 22q11.2, as well as duplications 7q11.23 and 16p11.2 [ 128 ].
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Detection of Morphological Abnormalities in Schizophrenia: An Important Step to Identify Associated Genetic Disorders or Etiologic Subtypes.
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