Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Learning and FMR1[original query] |
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| Confirmed rare copy number variants implicate novel genes in schizophrenia. Biochemical Society transactions 2010 Apr 38 (2): 445-51. Tam Gloria W C, van de Lagemaat Louie N, Redon Richard, Strathdee Karen E, Croning Mike D R, Malloy Mary P, Muir Walter J, Pickard Ben S, Deary Ian J, Blackwood Douglas H R, Carter Nigel P, Grant Seth G |
| A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis. Neurobiology of disease 2011 1 42 (1): 85-98. Qin Mei, Entezam Ali, Usdin Karen, Huang Tianjian, Liu Zhong-Hua, Hoffman Gloria E, Smith Carolyn |
| Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study. Biological psychiatry 2019 Apr 85 (7): 563-572. Silva Ana I, Ulfarsson Magnus O, Stefansson Hreinn, Gustafsson Omar, Walters G Bragi, Linden David E J, Wilkinson Lawrence S, Drakesmith Mark, Owen Michael J, Hall Jeremy, Stefansson Ka |
| Working memory and arithmetic impairments in children with FMR1 premutation and gray zone alleles. Dementia & neuropsychologia 2022 6 16 (1): 105-114. Martins Aline Aparecida Silva, Paiva Giulia Moreira, Matosinho Carolina Guimarães Ramos, Coser Elisângela Monteiro, Fonseca Pablo Augusto de Souza, Haase Vitor Geraldi, Carvalho Maria Raquel Sant |
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