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Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome
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 ...
Chelsea Lowther +2 more
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The 22q11.2 Deletion in Children
Journal of the American Academy of Child and Adolescent Psychiatry, 2006René Kahn +2 more
exaly
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome
Journal of Pediatrics, 2014Rita Consolini +2 more
exaly
Neuropsychiatric disorders in the 22q11 deletion syndrome
Genetics in Medicine, 2001Christopher Gillberg, Peder Rasmussen
exaly
22q11.2 Deletion syndrome is associated with perioperative outcome in tetralogy of Fallot
Journal of Thoracic and Cardiovascular Surgery, 2013Wei Yang +2 more
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