Showing results (421-430 of 442) with videos related to

Sort By:
Pageof 45
American Journal of Medical Genetics|March 26, 1998
Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired"W Yan, L K Jacobsen, D M Krasnewich, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Support for association between ADHD and two candidate genes: NET1 and DRD1Aaron J Bobb, Anjene M Addington, Ellen Sidransky, et al.
Neuroimage|October 27, 2004
Mapping cortical change in Alzheimer's disease, brain development, and schizophreniaPaul M Thompson, Kiralee M Hayashi, Elizabeth R Sowell, et al.
Clinical Breast Cancer|August 24, 2017
RESILIENCE: Phase III Randomized, Double-Blind Trial Comparing Sorafenib With Capecitabine Versus Placebo With Capecitabine in Locally Advanced or Metastatic HER2-Negative Breast CancerJosé Baselga, Claudio Zamagni, Patricia Gómez, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|February 11, 2010
A proposed EGFR inhibitor dermatologic adverse event-specific grading scale from the MASCC skin toxicity study groupMario E Lacouture, Michael L Maitland, Siegfried Segaert, et al.
European Journal of Cancer (Oxford, England : 1990)|September 16, 2025
Pharmacokinetics and bioavailability of pembrolizumab with berahyaluronidase alfa for subcutaneous administration in participants with advanced or metastatic solid tumors: The phase 1 study 3475A-C18Graham L Cohen, Corlia Coetzee, Cathryn A Walton, et al.
American Journal of Medical Genetics|December 20, 2000
Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21W L Yan, X Y Guan, E D Green, et al.
Molecular Psychiatry|December 21, 2011
Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disabilityL S Nguyen, L Jolly, C Shoubridge, et al.
Translational Psychiatry|July 27, 2012
Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophreniaJ Tarabeux, O Kebir, J Gauthier, et al.
Biological Psychiatry|July 22, 2010
De novo truncating mutation in Kinesin 17 associated with schizophreniaJulien Tarabeux, Nathalie Champagne, Edna Brustein, et al.
Pageof 45