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Neurology|December 15, 2004
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)J R M Oliveira, E Spiteri, M J Sobrido, et al.
American Journal of Human Genetics|July 9, 2013
Intellectual disability is associated with increased runs of homozygosity in simplex autismEce D Gamsiz, Emma W Viscidi, Abbie M Frederick, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|July 6, 2012
Sequential intra-arterial therapy and portal vein embolization is feasible and safe in patients with advanced hepatic malignanciesPeter D Peng, Omar Hyder, Mark Bloomston, et al.
Medrxiv : the Preprint Server for Health Sciences|October 14, 2024
Evaluating the Joint Effects of Recurrent Copy Number Variants and Polygenic Scores on the Risk of Psychiatric Disorders in the iPSYCH2015 Case-Cohort SampleMorteza Vaez, Simone Montalbano, Ryan Waples, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
A single cell multi-omic analysis identifies molecular and gene-regulatory mechanisms dysregulated in the developing Down syndrome neocortexCeline K Vuong, Alexis Weber, Patrick Seong, et al.
Acta Neuropathologica|December 5, 2022
Tuberous sclerosis complex is associated with a novel human tauopathyJi-Hye L Hwang, Olga S Perloff, Stephanie E Gaus, et al.
Nature Communications|November 17, 2021
Associations between patterns in comorbid diagnostic trajectories of individuals with schizophrenia and etiological factorsMorten Dybdahl Krebs, Gonçalo Espregueira Themudo, Michael Eriksen Benros, et al.
Eneurologicalsci|March 30, 2019
Validation of two parent-reported autism spectrum disorders screening tools M-CHAT-R and SCQ in Bamako, MaliModibo Sangare, Hamza B Toure, Amadou Toure, et al.
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