المؤلفون: Variants, Commission on Novel Technologies for Neurodevelopmental Copy Number, Buttermore, Elizabeth, Chamberlain, Stormy, Cody, Jannine, Costain, Gregory, Dang, Louis, DeWoody, Andrew, DeWoody, Yssa, Dies, Kira, Eichler, Evan, Girirajan, Santhosh, Gramm, Marie, Halladay, Alycia, Lal, Dennis, Lalli, Matthew, Levy, Tess, Logsdon, Glennis, Lowenstein, Daniel, Mefford, Heather, Mulle, Jennifer, Muotri, Alysson, Murphy, Melissa, Palma, Eduardo Perez, Pinter, Stefan, Pollak, Rebecca, Purcell, Ryan, Samaco, Rodney, Shah, Bina, Singh, Karun, So, Joyce, Sundberg, Maria, Veeraragavan, Surabi, Vogel-Farley, Vanessa, Wynshaw-Boris, Anthony

المصدر: American Journal of Human Genetics. 109(8)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Human Genome, Intellectual and Developmental Disabilities (IDD), Neurosciences, Brain Disorders, DNA Copy Number Variations, Genome, Humans, Neurodevelopmental Disorders, Patient Advocacy, Phenotype, Commission on Novel Technologies for Neurodevelopmental Copy Number Variants, CNVs, biobank, community engagement, copy-number variants, genomic disorders, iPSCs, inclusion, infrastructure, long-read sequencing, neurodevelopment, neurological, patient centered, patient led, structural variants, systematic phenotyping, team science, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3tc3h13fTest

المؤلفون: Commission on Novel Technologies for Neurodevelopmental Copy Number Variants

المصدر: American journal of human genetics, vol 109, iss 8

مصطلحات موضوعية: DNA Copy Number Variations, systematic phenotyping, Intellectual and Developmental Disabilities (IDD), Commission on Novel Technologies for Neurodevelopmental Copy Number Variants, iPSCs, Patient Advocacy, community engagement, infrastructure, Medical and Health Sciences, patient centered, team science, Genetics, Humans, genomic disorders, CNVs, Genetics & Heredity, neurological, Genome, neurodevelopment, Human Genome, Neurosciences, structural variants, Biological Sciences, Brain Disorders, biobank, Phenotype, copy-number variants, inclusion, Neurodevelopmental Disorders, patient led, long-read sequencing

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_______325::cd8f9d889d382bba628948109c91d0b8Test
https://escholarship.org/uc/item/3tc3h13fTest