Fragile x syndrome|https://phgkb.cdc.gov/GAPPKB/phgHome.do|Fragile x syndrome

https://phgkb.cdc.gov/GAPPKB/phgHome.do

From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• 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

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