Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and MYT1L[original query] |
---|
Association study of myelin transcription factor 1-like polymorphisms with schizophrenia in Han Chinese population. Genes, brain, and behavior 2012 Feb 11 (1): 87-93. Li W, Wang X, Zhao J, Lin J, Song X-Q, Yang Y, Jiang C, Xiao B, Yang G, Zhang H-X, Lv L |
Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system. Pain 2014 Jun 155 (6): 1102-9. Docampo Elisa, Escaramís Georgia, Gratacòs Mònica, Villatoro Sergi, Puig Anna, Kogevinas Manolis, Collado Antonio, Carbonell Jordi, Rivera Javier, Vidal Javier, Alegre Jose, Estivill Xavier, Rabionet Raqu |
Copy number variation in a hospital-based cohort of children with epilepsy. Epilepsia open 2017 Jun 2 (2): 244-254. Vlaskamp Danique R M, Callenbach Petra M C, Rump Patrick, Giannini Lucia A A, Dijkhuizen Trijnie, Brouwer Oebele F, van Ravenswaaij-Arts Conny M |
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 |
A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study.
Scientific reports 2021 5 11 (1): 9446. Yoshimura Keito, Morita Yuji, Konomi Kenji, Ishida Sachiko, Fujiwara Daisuke, Kobayashi Keisuke, Tanaka Masa |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: