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1دورية أكاديمية
المؤلفون: Bell, Kathleen Anne, Kim, Raymond, Aronson, Melyssa, Gillies, Brittany, Ali Awan, Arif, Chun, Kathy, Hart, Jennifer, Healey, Rachel, Kim, Linda, Klaric, Goran, Panabaker, Karen, Sabatini, Peter J B, Sadikovic, Bekim, Selvarajah, Shamini, Smith, Amanda C, Stockley, Tracy L, Vaags, Andrea K, Eisen, Andrea, Pollett, Aaron, Feilotter, Harriet
مصطلحات موضوعية: Cancer genetics
وصف الملف: text/html
العلاقة: http://jmg.bmj.com/cgi/content/short/60/8/769Test; http://dx.doi.org/10.1136/jmg-2022-108945Test
الإتاحة: https://doi.org/10.1136/jmg-2022-108945Test
http://jmg.bmj.com/cgi/content/short/60/8/769Test -
2دورية أكاديمية
المؤلفون: Grafodatskaya, Daria, O’Rielly, Darren D, Bedard, Karine, Butcher, Darci T, Howlett, Christopher J, Lytwyn, Alice, McCready, Elizabeth, Parboosingh, Jillian, Spriggs, Elizabeth L, Vaags, Andrea K, Stockley, Tracy L
المصدر: Journal of Medical Genetics ; volume 59, issue 8, page 727-736 ; ISSN 0022-2593 1468-6244
مصطلحات موضوعية: Genetics (clinical), Genetics
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3دورية أكاديمية
المؤلفون: Chénier, Sébastien, Yoon, Grace, Argiropoulos, Bob, Lauzon, Julie, Laframboise, Rachel, Ahn, Joo Wook, Ogilvie, Caroline Mackie, Lionel, Anath C, Marshall, Christian R, Vaags, Andrea K, Hashemi, Bita, Boisvert, Karine, Mathonnet, Géraldine, Tihy, Frédérique, So, Joyce, Scherer, Stephen W, Lemyre, Emmanuelle, Stavropoulos, Dimitri J
المصدر: Journal of Neurodevelopmental Disorders. 6(1)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Genetics, Intellectual and Developmental Disabilities (IDD), Mental Health, Brain Disorders, Human Fetal Tissue, Pediatric, Biotechnology, Autism, Aetiology, 2.1 Biological and endogenous factors, Neurological, Mental health, Autism spectrum disorder, CHD2, Developmental delay, Epilepsy, Learning disability, Psychology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/1kr700gvTest
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4دورية أكاديمية
المؤلفون: Lionel, Anath C, Tammimies, Kristiina, Vaags, Andrea K, Rosenfeld, Jill A, Ahn, Joo Wook, Merico, Daniele, Noor, Abdul, Runke, Cassandra K, Pillalamarri, Vamsee K, Carter, Melissa T, Gazzellone, Matthew J, Thiruvahindrapuram, Bhooma, Fagerberg, Christina, Laulund, Lone W, Pellecchia, Giovanna, Lamoureux, Sylvia, Deshpande, Charu, Clayton-Smith, Jill, White, Ann C, Leather, Susan, Trounce, John, Bedford, H Melanie, Hatchwell, Eli, Eis, Peggy S, Yuen, Ryan KC, Walker, Susan, Uddin, Mohammed, Geraghty, Michael T, Nikkel, Sarah M, Tomiak, Eva M, Fernandez, Bridget A, Soreni, Noam, Crosbie, Jennifer, Arnold, Paul D, Schachar, Russell J, Roberts, Wendy, Paterson, Andrew D, So, Joyce, Szatmari, Peter, Chrysler, Christina, Woodbury-Smith, Marc, Lowry, R Brian, Zwaigenbaum, Lonnie, Mandyam, Divya, Wei, John, MacDonald, Jeffrey R, Howe, Jennifer L, Nalpathamkalam, Thomas, Wang, Zhuozhi, Tolson, Daniel, Cobb, David S, Wilks, Timothy M, Sorensen, Mark J, Bader, Patricia I, An, Yu, Wu, Bai-Lin, Musumeci, Sebastiano Antonino, Romano, Corrado, Postorivo, Diana, Nardone, Anna M, Della Monica, Matteo, Scarano, Gioacchino, Zoccante, Leonardo, Novara, Francesca, Zuffardi, Orsetta, Ciccone, Roberto, Antona, Vincenzo, Carella, Massimo, Zelante, Leopoldo, Cavalli, Pietro, Poggiani, Carlo, Cavallari, Ugo, Argiropoulos, Bob, Chernos, Judy, Brasch-Andersen, Charlotte, Speevak, Marsha, Fichera, Marco, Ogilvie, Caroline Mackie, Shen, Yiping, Hodge, Jennelle C, Talkowski, Michael E, Stavropoulos, Dimitri J, Marshall, Christian R, Scherer, Stephen W
المصدر: Human Molecular Genetics. 23(10)
مصطلحات موضوعية: Pediatric Research Initiative, Pediatric, Intellectual and Developmental Disabilities (IDD), Mental Health, Brain Disorders, Human Genome, Neurosciences, Autism, Clinical Research, Behavioral and Social Science, Genetics, 2.1 Biological and endogenous factors, Aetiology, Mental health, Adolescent, Adult, Attention Deficit Disorder with Hyperactivity, Case-Control Studies, Child, Child Development Disorders, Pervasive, Child, Preschool, Chromosomes, Human, Pair 9, DNA Copy Number Variations, Exons, Female, Gene Expression, Genetic Association Studies, Genetic Predisposition to Disease, Glycoproteins, Humans, Infant, Infant, Newborn, Male, Nerve Tissue Proteins, Organ Specificity, Phenotype, Polymorphism, Single Nucleotide, Protein Isoforms, Receptors, Cell Surface, Risk Factors, Sequence Deletion, Transcription Factors, Transcription Initiation Site, Tripartite Motif Proteins, Ubiquitin-Protein Ligases, Young Adult, Biological Sciences, Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/59x2g1gfTest
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5دورية أكاديمية
المؤلفون: Bell, Kathleen Anne, Kim, Raymond, Aronson, Melyssa, Gillies, Brittany, Ali Awan, Arif, Chun, Kathy, Hart, Jennifer, Healey, Rachel, Kim, Linda, Klaric, Goran, Panabaker, Karen, Sabatini, Peter J B, Sadikovic, Bekim, Selvarajah, Shamini, Smith, Amanda C, Stockley, Tracy L, Vaags, Andrea K, Eisen, Andrea, Pollett, Aaron, Feilotter, Harriet
المصدر: Journal of Medical Genetics ; volume 60, issue 8, page 769-775 ; ISSN 0022-2593 1468-6244
مصطلحات موضوعية: Genetics (clinical), Genetics
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6دورية أكاديمية
المؤلفون: Addis, Laura, Ahn, Joo Wook, Dobson, Richard, Dixit, Abhishek, Ogilvie, Caroline M, Pinto, Dalila, Vaags, Andrea K, Coon, Hilary, Chaste, Pauline, Wilson, Scott, Parr, Jeremy R, Andrieux, Joris, Lenne, Bruno, Tumer, Zeynep, Leuzzi, Vincenzo, Aubell, Kristina, Koillinen, Hannele, Curran, Sarah, Marshall, Christian R, Scherer, Stephen W, Strug, Lisa J, Collier, David A, Pal, Deb K
مصطلحات موضوعية: Genetics (clinical), Genetics, European Commission
العلاقة: info:eu-repo/grantAgreement/EC/FP7/602531/; url:https://www.openaccessrepository.it/communities/itmirrorTest; https://www.openaccessrepository.it/record/190322Test
الإتاحة: https://doi.org/10.1002/humu.22816Test
https://www.openaccessrepository.it/record/190322Test -
7دورية أكاديمية
المؤلفون: Mighton, Chloe, Smith, Amanda C, Mayers, Justin, Tomaszewski, Robert, Taylor, Sherryl, Hume, Stacey, Agatep, Ron, Spriggs, Elizabeth, Feilotter, Harriet E, Semenuk, Laura, Wong, Henry, Lazo de la Vega, Lorena, Marshall, Christian R, Axford, Michelle M, Silver, Talia, Charames, George S, Di Gioacchino, Vanessa, Watkins, Nicholas, Foulkes, William D, Clavier, Marcos, Hamel, Nancy, Chong, George, Lamont, Ryan E, Parboosingh, Jillian, Karsan, Aly, Bosdet, Ian, Young, Sean S, Tucker, Tracy, Akbari, Mohammad Reza, Speevak, Marsha D, Vaags, Andrea K, Lebo, Matthew S, Lerner-Ellis, Jordan
المساهمون: Ontario Genomics Institute, Canadian Institutes of Health Research
المصدر: Journal of Medical Genetics ; volume 59, issue 6, page 571-578 ; ISSN 0022-2593 1468-6244
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8دورية أكاديمية
المؤلفون: Krutikov, Konstantin, Zheng, Yanzhen, Chesney, Alden, Huang, Xiaoyong, Vaags, Andrea K., Evdokimova, Valentina, Hough, Margaret R., Chen, Edwin
المساهمون: Rishi, Arun
المصدر: PLoS ONE ; volume 9, issue 2, page e89649 ; ISSN 1932-6203
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9دورية أكاديمية
المؤلفون: Mattman, Andre, Gilfix, Brian M., Chen, Sharon Xuehui, DeMarco, Mari L., Kyle, Barry D., Parker, Michelle L., Agbor, Terence A., Jung, Benjamin, Selvarajah, Shamini, Barakauskas, Vilte E., Vaags, Andrea K., Estey, Mathew P., Nelson, Tanya N., Speevak, Marsha D.
المصدر: Clinical Biochemistry ; volume 81, page 27-33 ; ISSN 0009-9120
مصطلحات موضوعية: Clinical Biochemistry, General Medicine
الإتاحة: https://doi.org/10.1016/j.clinbiochem.2020.05.001Test
https://api.elsevier.com/content/article/PII:S000991202030076X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S000991202030076X?httpAccept=text/plainTest -
10دورية أكاديمية
المؤلفون: Handrigan, Gregory Ryan, Chitayat, David, Lionel, Anath C, Pinsk, Maury, Vaags, Andrea K, Marshall, Christian R, Dyack, Sarah, Escobar, Luis F, Fernandez, Bridget A, Stegman, Joseph C, Rosenfeld, Jill A, Shaffer, Lisa G, Goodenberger, McKinsey, Hodge, Jennelle C, Cain, Jason E, Babul-Hirji, Riyana, Stavropoulos, Dimitri J, Yiu, Verna, Scherer, Stephen W, Rosenblum, Norman D
مصطلحات موضوعية: Copy-number variation
وصف الملف: text/html
العلاقة: http://jmg.bmj.com/cgi/content/short/50/3/163Test; http://dx.doi.org/10.1136/jmedgenet-2012-101288Test
الإتاحة: https://doi.org/10.1136/jmedgenet-2012-101288Test
http://jmg.bmj.com/cgi/content/short/50/3/163Test