Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: CNTN3[original query] |
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Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association. Journal of vascular surgery 2009 Jun 49 (6): 1525-31. Elmore James R, Obmann Melissa A, Kuivaniemi Helena, Tromp Gerard, Gerhard Glenn S, Franklin David P, Boddy Amy M, Carey David |
CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders. Journal of neurodevelopmental disorders 2015 7 (1): 26. Hu Jie, Liao Jun, Sathanoori Malini, Kochmar Sally, Sebastian Jessica, Yatsenko Svetlana A, Surti Urvas |
Pharmacogenetics of dipeptidyl peptidase 4 inhibitors in a Taiwanese population with type 2 diabetes. Oncotarget 2017 Mar 8 (11): 18050-18058. Liao Wen-Ling, Lee Wen-Jane, Chen Ching-Chu, Lu Chieh Hsiang, Chen Chien-Hsiun, Chou Yi-Chun, Lee I-Te, Sheu Wayne H-H, Wu Jer-Yuarn, Yang Chi-Fan, Wang Chung-Hsing, Tsai Fuu-J |
Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing. International journal of legal medicine 2018 7 132 (5): 1273-1280. Zheng Jinxiang, Guo Jian, Huang Lei, Wu Qiuping, Yin Kun, Wang Lin, Zhang Tongda, Quan Li, Zhao Qianhao, Cheng Jiandi |
Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study.
Molecular biology reports 2020 Oct 47 (10): 7623-7632. Alsubaie Laila M, Alsuwat Hind Saleh, Almandil Noor B, AlSulaiman Abdulla, AbdulAzeez Sayed, Borgio J Franc |
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