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Reply: ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.
Common and specific transcriptional signatures in mouse embryos and adult tissues induced by in vitro procedures.
Early Predictors of Impaired Social Functioning in Male Rhesus Macaques (Macaca mulatta).
Dendritic cell sphingosine-1-phosphate lyase regulates thymic egress.
Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum.
278 Emergency Department Utilization by Californians With Sickle Cell Disease, 2005-2014.
Combining Prognostic and Predictive Enrichment Strategies to Identify Children With Septic Shock Responsive to Corticosteroids.
Bedside Ultrasound for Tracheal Tube Verification in Pediatric Emergency Department and ICU Patients: A Systematic Review.
Rooted in risk: genetic predisposition for low-density lipoprotein cholesterol level associates with diminished low-density lipoprotein cholesterol response to statin treatment.
Characterizing cognitive control abilities in children with 16p11.2 deletion using adaptive 'video game' technology: a pilot study.