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Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia

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Year: 2007
Type: article
Study design: Observational Study
Source: Schizophrenia Research
DOI: 10.1016/j.schres.2007.09.025
Authors: Mechteld L.C. Hoogendoorn, Jacob A.S. Vorstman, Gholam R. Jalali, Jean-Paul Selten, Richard J. Sinke, Beverly S. Emanuel, René S. Kahn
Institutions: University Medical Center Utrecht, Children's Hospital of Philadelphia
Language: English

Topic: Schizophrenia research and treatment
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: green

Funders: National Alliance for Research on Schizophrenia and Depression, National Heart, Lung, and Blood Institute, National Cancer Institute
Awards: Genetic Modifiers for 22q 11.2 Deletion Syndrome, Cytogenetic and Molecular Studies of Chromosome 22
OpenAlex ID: W2114726224
FWCI: 2.813
Cites: 33
Cited by: 36
Related to: 10
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