Author:
Parker David Alan,Imes Sid,Ruban Gabrielle,Ousley Opal Yates,Henshey Brett,Massa Nicholas M.,Walker Elaine,Cubells Joseph F.,Duncan Erica
Funder
NIMH
NCATS
Department of Psychiatry and Behavioral Sciences, School of Medicine, Stanford University
School of Medicine, Emory University
National Institutes of Health
Reference87 articles.
1. Genetic influences on prepulse inhibition of startle reflex in humans;Anokhin;Neurosci. Lett.,2003
2. The schizophrenia phenotype in 22q11 deletion syndrome;Bassett;Am. J. Psychiatry,2003
3. Clinical features of 78 adults with 22q11 deletion syndrome;Bassett;Am. J. Med. Genet. A,2005
4. Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening;Blagojevic;Canad. Med. Assoc. J. Open,2021
5. Committee report: guidelines for human startle eyeblink electromyographic studies;Blumenthal;Psychophysiology,2005