Detection Of Risk Genes For Psychosis In A Family With 22Q11.2ds - Preliminary Findings
Sign Up to like & getrecommendations! Published in 2017 at "European Neuropsychopharmacology"
DOI: 10.1016/j.euroneuro.2016.09.569
Abstract: Abstract The 22q11.2 deletion syndrome (22q11.2DS) is the most common microdeletion syndrome in humans. It is a multisystem congenital anomaly disorder characterized by variable manifestations including high rates of neuropsychiatric disorders. A unique 22q11.2DS multigeneration… read more here.
Keywords: 22q11 2ds; detection risk; family; haplotype ... See more keywords