Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome
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DOI: 10.1007/s11920-021-01225-z
Abstract: The 22q11.2 deletion syndrome (22q11DS) is associated with a broad spectrum of neurodevelopmental phenotypes and is the strongest known single genetic risk factor for schizophrenia. Compared to other rare structural pathogenic genetic variants, 22q11DS is… read more here.
Keywords: deletion syndrome; trajectories psychiatric; neurodevelopmental phenotypes; neurodevelopmental trajectories ... See more keywords