Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and FOXP2[original query] |
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Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European journal of human genetics : EJHG 2009 Oct 17 (10): 1354-8. Vernes Sonja C, MacDermot Kay D, Monaco Anthony P, Fisher Simon |
Etiological yield of SNP microarrays in idiopathic intellectual disability. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2014 May 18 (3): 327-37. Utine G Eda, Halilo?lu Göknur, Volkan-Salanc? Bilge, Çetinkaya Arda, Kiper Pelin Ö, Alanay Yasemin, Akta? Dilek, Anlar Banu, Topçu Meral, Boduro?lu Koray, Alika?ifo?lu Mehm |
Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population. Journal of neural transmission (Vienna, Austria : 1996) 2017 Apr . Rao Wenwang, Du Xiangdong, Zhang Yingyang, Yu Qiong, Hui Li, Yu Yaqin, Kou Changgui, Yin Guangzhong, Zhu Xiaomin, Man Lijuan, Soares Jair C, Zhang Xiang Ya |
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS genetics 2018 12 14 (12): e1007535. Toma Claudio, Pierce Kerrie D, Shaw Alex D, Heath Anna, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
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