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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 2, 2023. (Total: 221654Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: TBR1[original query]
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
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