From HuGE Literature Finder Database: Fragile X Syndrome || Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)

From HuGE Literature Finder Database

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

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• 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
• The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder.
  Scientific reports 2016 6 19372.
  Wenger Tara L, Kao Charlly, McDonald-McGinn Donna M, Zackai Elaine H, Bailey Alice, Schultz Robert T, Morrow Bernice E, Emanuel Beverly S, Hakonarson Hak
• Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP Haplotype.
  Genetics research international 2016 2016 8319287.
  Limprasert Pornprot, Thanakitgosate Janpen, Jaruthamsophon Kanoot, Sripo Than

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