المؤلفون: Cody, Jannine D.^{Aff3, Aff4}

المساهمون: Li, Peining, editor^Aff1, Liehr, Thomas, editor^Aff2

المصدر: Human Ring Chromosomes : A Practical Guide for Clinicians and Families. :261-270

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

URL الوصول: https://escholarship.org/uc/item/3tc3h13f

المؤلفون: 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, Perez Palma, Eduardo, 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: In The American Journal of Human Genetics 4 August 2022 109(8):1353-1365

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المؤلفون: Mehl, Justin M., Gelfond, Jonathan, Carey, John C., Cody, Jannine D.

المصدر: American Journal of Medical Genetics. Part A; Feb2024, Vol. 194 Issue 2, p279-287, 9p

المؤلفون: Cody, Jannine D.^{Aff1, Aff2}, Heard, Patricia, Rupert, David, Hasi-Zogaj, Minire, Hill, Annice, Sebold, Courtney, Hale, Daniel E.^{Aff1, Aff3}

المصدر: Human Genetics. 137(11-12):961-970

المؤلفون: Cody, Jannine D.^{Aff1, Aff2}

المصدر: Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 22(1):234-235

المؤلفون: Carey, John, Cody, Jannine, Mehl, Justin, Gelfond, Jonathan

المصدر: In Genetics in Medicine Open 2023 1(1) Supplement

المؤلفون: Soileau, Bridgette, Hasi, Minire, Sebold, Courtney, Hill, Annice, O’Donnell, Louise, Hale, Daniel E., Cody, Jannine D.

المصدر: Journal of Genetic Counseling. August 2015 24(4):663-674