Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: DIP2C[original query] |
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A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.
Obesity (Silver Spring, Md.) 2013 Jan . Li WD, Jiao H, Wang K, Zhang CK, Glessner JT, Grant SF, Zhao H, Hakonarson H, Arlen Price R |
Intragenic Deletion of the ZMYND11 Gene in 10p15.3 is Associated with Developmental Delay Phenotype: A Case Report. Cytogenetic and genome research 2021 11 161 (8-9): 445-448. Huynh Minh-Tuan, Tran Cong Toai, Joubert Madeleine, Bénéteau Clai |
DIP2C polymorphisms are implicated in susceptibility and clinical phenotypes of autism spectrum disorder. Psychiatry research 2022 Oct 316 114792. Li Yan, Sun Chuanyong, Guo Yanbo, Qiu Shuang, Li Yong, Liu Yunkai, Zhong Weijing, Wang Hedi, Cheng Yi, Liu Yaw |
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder. Human genetics 2024 2 . Ashraf Yahia, Danyang Li, Sanna Lejerkrans, Shyam Rajagopalan, Nelli Kalnak, Kristiina Tammimi |
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- Page last updated:Apr 22, 2024
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