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Results 1 - 10 of 26 for Schizophrenia 3
  1. ... with an increased risk of psychiatric disorders, particularly schizophrenia. Other signs and symptoms of 15q13.3 microdeletion can include heart defects, minor abnormalities involving ...
  2. ... Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. PLoS Genet. 2016 May 6; ...
  3. ... of patients diagnosed with schizoaffective disorder compared with schizophrenia and bipolar disorder. Bipolar Disord. 2013 May;15(3):229-39. doi: 10.1111/bdi.12057. Epub ...
  4. ... channels are under study for the treatment of schizophrenia, Alzheimer's disease, and pain. At least three mutations in the CHRNB2 gene have been identified ...
  5. ... and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network. Cell. 2013 Aug 1;154(3):518-29. doi: 10.1016/j.cell.2013. ...
  6. ... a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies. Am J Psychiatry. 2003 Mar;160(3):469-76. doi: 10.1176/appi.ajp.160. ...
  7. ... of behavioral problems and mental illness such as schizophrenia (described below). Most people with 22q11.2 deletion syndrome are missing about 3 million base pairs on one copy of chromosome ...
  8. ... This Health Condition MedlinePlus Genetics provides ... instructions are used to make the 14-3-3 epsilon protein, while others delete some or ...
  9. ... behavioral abnormalities. 1q21.1 microduplications occur in about 3 in 10,000 individuals in the general population. Studies suggest that these chromosomal changes are 15 to 20 times more common in people with schizophrenia or tetralogy of Fallot. Many people with 1q21. ...
  10. ... with FFEVF have developed psychiatric disorders (such as schizophrenia), behavioral problems, or ... in the NPRL2 or NPRL3 gene. These three genes provide instructions for making proteins that attach ( ...
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