Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Mental Retardation and FOXG1[original query] |
---|
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant. Neurogenetics 2010 May 11 (2): 241-9. Bahi-Buisson Nadia, Nectoux Juliette, Girard Benoit, Van Esch Hilde, De Ravel Thomy, Boddaert Nathalie, Plouin Perrine, Rio Marlene, Fichou Yann, Chelly Jamel, Bienvenu Thier |
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation. BMC medical genetics 2017 8 18 (1): 96. Zhang Qingping, Wang Jiaping, Li Jiarui, Bao Xinhua, Zhao Ying, Zhang Xiaoying, Wei Liping, Wu Xi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Jun 11, 2024
- Content source: