المؤلفون: Marc Woodbury-Smith, E. Robert Wassman, Nadeem Murtaza, James Stavropoulos, Stephen W. Scherer, Erin Harward, Vickie Kwan, Sylvia Lamoureux, Biren M. Dave, Leon Chalil, Marsha Speevak, Nicholas Holzapfel, Lia D’Abate, Sean H. White, Jacob Nielsen, Mohammed Uddin, Thomas Nalpathamkalam, Brad Doble, Karun K. Singh, John Wei, Kristin J Hope, Giovanna Pellecchia, Brianna K. Unda, Karen S. Ho

المصدر: American Journal of Human Genetics

مصطلحات موضوعية: 0301 basic medicine, Male, Dendritic spine, Autism Spectrum Disorder, Dendritic Spines, Chromosome Disorders, OTUD7A, Biology, Article, dendrite, Transcriptome, 03 medical and health sciences, Mice, 0302 clinical medicine, Neurodevelopmental disorder, Prosencephalon, Seizures, synapse, Intellectual Disability, Endopeptidases, Genetics, medicine, Animals, Humans, Copy-number variation, Genetics (clinical), Genetic Association Studies, Chromosomes, Human, Pair 15, Deubiquitinating Enzymes, dendritic spine, Human brain, Microdeletion syndrome, medicine.disease, neurodevelopmental disorder, schizophrenia, deubiquitinase, 030104 developmental biology, medicine.anatomical_structure, Phenotype, copy-number variation, Autism spectrum disorder, Schizophrenia, Neurodevelopmental Disorders, 15q13.3 microdeletion syndrome, Female, Chromosome Deletion, Neuroscience, 030217 neurology & neurosurgery, Gene Deletion

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe1b0e101470cca83445b2de71df3227
https://pubmed.ncbi.nlm.nih.gov/29395074

المؤلفون: Moises A. Serrano, Rena Vanzo, Karen S. Ho, Megan M. Martin, Hope Twede, E. Robert Wassman, Patricia Mowery-Rushton, Stephanie Page, Erin Harward, Andreas Peiffer, Charles H. Hensel

المصدر: BioMed Research International, Vol 2016 (2016)
BioMed Research International

مصطلحات موضوعية: 0301 basic medicine, Male, Pediatrics, medicine.medical_specialty, Article Subject, Microarray, Adolescent, Autism Spectrum Disorder, Developmental Disabilities, Gene Dosage, lcsh:Medicine, General Biochemistry, Genetics and Molecular Biology, Chromosomes, Cohort Studies, 03 medical and health sciences, Young Adult, Intellectual Disability, Intellectual disability, mental disorders, medicine, Chromosomes, Human, Humans, Copy-number variation, Child, Oligonucleotide Array Sequence Analysis, Chromosome Aberrations, General Immunology and Microbiology, business.industry, Clinical Laboratory Techniques, lcsh:R, Genetic Variation, General Medicine, medicine.disease, 030104 developmental biology, Ultrahigh resolution, Autism spectrum disorder, Neurodevelopmental Disorders, Child, Preschool, Karyotyping, Cohort, Etiology, Female, business, Cohort study, Research Article

وصف الملف: text/xhtml

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee2f1cd1548a295f4cd8b2471d1d9d85
https://doaj.org/article/b0ac558de9a24d41883c9f5834edfb7f