Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: TBR1[original query] |
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De novo mutations in moderate or severe intellectual disability. PLoS genetics 2014 Oct 10 (10): e1004772. Hamdan Fadi F, Srour Myriam, Capo-Chichi Jose-Mario, Daoud Hussein, Nassif Christina, Patry Lysanne, Massicotte Christine, Ambalavanan Amirthagowri, Spiegelman Dan, Diallo Ousmane, Henrion Edouard, Dionne-Laporte Alexandre, Fougerat Anne, Pshezhetsky Alexey V, Venkateswaran Sunita, Rouleau Guy A, Michaud Jacques |
Microsatellite polymorphisms associated with human behavioural and psychological phenotypes including a gene-environment interaction. BMC medical genetics 2017 Feb 18 (1): 12. Bagshaw Andrew T M, Horwood L John, Fergusson David M, Gemmell Neil J, Kennedy Martin |
An Intronic Variant of CHD7 Identified in Autism Patients Interferes with Neuronal Differentiation and Development. Neuroscience bulletin 2021 5 37 (8): 1091-1106. Zhang Ran, He Hui, Yuan Bo, Wu Ziyan, Wang Xiuzhen, Du Yasong, Chen Yuejun, Qiu Zilo |
Identification and Potential Clinical Utility of Common Genetic Variants in Gestational Diabetes among Chinese Pregnant Women. Diabetes & metabolism journal 2024 9 . Claudia Ha-Ting Tam, Ying Wang, Chi Chiu Wang, Lai Yuk Yuen, Cadmon King-Poo Lim, Junhong Leng, Ling Wu, Alex Chi-Wai Ng, Yong Hou, Kit Ying Tsoi, Hui Wang, Risa Ozaki, Albert Martin Li, Qingqing Wang, Juliana Chung-Ngor Chan, Yan Chou Ye, Wing Hung Tam, Xilin Yang, Ronald Ching-Wan |
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