- Gene-set analysis shows association between FMRP targets and autism spectrum disorder.
European journal of human genetics : EJHG 2017 Apr .
Jansen Arija, Dieleman Gwen C, Smit August B, Verhage Matthijs, Verhulst Frank C, Polderman Tinca J C, Posthuma Daniel
- Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome.
Brain & development 2017 Feb .
AlOlaby Reem Rafik, Sweha Stefan R, Silva Marisol, Durbin-Johnson Blythe, Yrigollen Carolyn M, Pretto Dalyir, Hagerman Randi J, Tassone Flo
- Distribution of the FMR1 gene in females by race/ethnicity: women with diminished ovarian reserve versus women with normal fertility (SWAN study).
Fertility and sterility 2016 Nov .
Pastore Lisa M, Young Steven L, Manichaikul Ani, Baker Valerie L, Wang Xin Q, Finkelstein Joel
- Contraction of fully expanded FMR1 alleles to the normal range: predisposing haplotype or rare events?
Journal of human genetics 2016 Oct .
Maia Nuno, Loureiro Joana R, Oliveira Bárbara, Marques Isabel, Santos Rosário, Jorge Paula, Martins Sand
- [SNP array and cytogenetic analysis of a patient with unexplained mental retardation].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 Jun 33 (3): 332-4.
Bai Nan, Mei Shiyue, Zhao Zhenhua, Kong Xiangdo
domingo, 16 de julio de 2017
Fragile x syndrome | Updates on Specific Diseases
From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology