Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: SAE1[original query] |
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A discovery resource of rare copy number variations in individuals with autism spectrum disorder. G3 (Bethesda, Md.) 2012 Dec 2 (12): 12. Prasad A, Merico D, Thiruvahindrapuram B, Wei J, Lionel AC, Sato D, Rickaby J, Lu C, Szatmari P, Roberts W, Fernandez BA, Marshall CR, Hatchwell E, Eis PS, Scherer SW |
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA. American journal of human genetics 2016 Jan 98 (1): 58-74. Turner Tychele N, Hormozdiari Fereydoun, Duyzend Michael H, McClymont Sarah A, Hook Paul W, Iossifov Ivan, Raja Archana, Baker Carl, Hoekzema Kendra, Stessman Holly A, Zody Michael C, Nelson Bradley J, Huddleston John, Sandstrom Richard, Smith Joshua D, Hanna David, Swanson James M, Faustman Elaine M, Bamshad Michael J, Stamatoyannopoulos John, Nickerson Deborah A, McCallion Andrew S, Darnell Robert, Eichler Evan |
The spectrum and clinical significance of myositis-specific autoantibodies in Chinese patients with idiopathic inflammatory myopathies. Clinical rheumatology 2019 Mar . Li Shanshan, Ge Yongpeng, Yang Hanbo, Wang Tao, Zheng Xiaoxiao, Peng Qinglin, Lu Xin, Wang Guoch |
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- Page last updated:May 13, 2024
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