Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and MYT1L[original query] |
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| Recurrent CNVs disrupt three candidate genes in schizophrenia patients. American journal of human genetics 2008 Oct 83 (4): 504-10. Vrijenhoek Terry, Buizer-Voskamp Jacobine E, van der Stelt Inge, Strengman Eric, , Sabatti Chiara, Geurts van Kessel Ad, Brunner Han G, Ophoff Roel A, Veltman Joris |
A genome-wide association study of brain lesion distribution in multiple sclerosis.
Brain : a journal of neurology 2013 Apr 136 (Pt 4): 1012-24. Gourraud Pierre-Antoine, Sdika Michael, Khankhanian Pouya, Henry Roland G, Beheshtian Azadeh, Matthews Paul M, Hauser Stephen L, Oksenberg Jorge R, Pelletier Daniel, Baranzini Sergio |
| Genome-Wide Variants Associated With Longitudinal Survival Outcomes Among Individuals With Coronary Artery Disease. Frontiers in genetics 2021 12 661497. Dungan Jennifer R, Qin Xue, Hurdle Melissa, Haynes Carol S, Hauser Elizabeth R, Kraus William |
| Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
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