Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Abnormalities and SHANK3[original query] |
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Association study of SHANK3 gene polymorphisms with autism in Chinese Han population. BMC medical genetics 2009 10 61. Qin Jian, Jia Meixiang, Wang Lifang, Lu Tianlan, Ruan Yan, Liu Jing, Guo Yanqing, Zhang Jishui, Yang Xiaoling, Yue Weihua, Zhang D |
[Prenatal genetic analysis of three fetuses with abnormalities of chromosome 22]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 3 37 (4): 405-409. Ge Yunsheng, Zhang Jian, Cai Meijiao, Chen Xiaolu, Zhou Yul |
A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes. Orphanet journal of rare diseases 2020 12 15 (1): 335. Xu Na, Lv Hui, Yang Tingting, Du Xiujuan, Sun Yu, Xiao Bing, Fan Yanjie, Luo Xiaomei, Zhan Yongkun, Wang Lili, Li Fei, Yu Yongg |
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium. Human molecular genetics 2021 9 31 (4): 625-637. Levy Tess, Foss-Feig Jennifer H, Betancur Catalina, Siper Paige M, Trelles-Thorne Maria Del Pilar, Halpern Danielle, Frank Yitzchak, Lozano Reymundo, Layton Christina, Britvan Bari, Bernstein Jonathan A, Buxbaum Joseph D, Berry-Kravis Elizabeth, Powell Craig M, Srivastava Siddharth, Sahin Mustafa, Soorya Latha, Thurm Audrey, Kolevzon Alexander, |
Sensory Reactivity Phenotype in Phelan-McDermid Syndrome Is Distinct from Idiopathic ASD. Genes 2021 Jun 12 (7): . Tavassoli Teresa, Layton Christina, Levy Tess, Rowe Mikaela, George-Jones Julia, Zweifach Jessica, Lurie Stacey, Buxbaum Joseph D, Kolevzon Alexander, Siper Paige |
Sleep Duration in Mouse Models of Neurodevelopmental Disorders. Brain sciences 2021 1 11 (1): . Saré Rachel Michelle, Lemons Abigail, Song Alex, Smith Carolyn Bee |
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- Page last updated:Jun 02, 2023
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