Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and meta-analysis and IMMP2L[original query] |
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Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Frontiers in neuroscience 2016 10 531. Padmanabhuni Shanmukha S, Houssari Rayan, Esserlind Ann-Louise, Olesen Jes, Werge Thomas M, Hansen Thomas F, Bertelsen Birgitte, Tsetsos Fotis, Paschou Peristera, Tümer Zeyn |
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Nov . Zhang Yanqing, Liu Yi, Zarrei Mehdi, Tong Winnie, Dong Rui, Wang Ying, Zhang Haiyan, Yang Xiaomeng, MacDonald Jeffrey R, Uddin Mohammed, Scherer Stephen W, Gai Zhongt |
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome. Frontiers in neurology 2020 9 11 803. Pagliaroli Luca, Vereczkei Andrea, Padmanabhuni Shanmukha Sampath, Tarnok Zsanett, Farkas Luca, Nagy Peter, Rizzo Renata, Wolanczyk Tomasz, Szymanska Urszula, Kapisyzi Mira, Basha Entela, Koumoula Anastasia, Androutsos Christos, Tsironi Vaia, Karagiannidis Iordanis, Paschou Peristera, Barta Csa |
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