Early Identification of Fragile X Syndrome through Expanded Newborn Screening

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Last Posted: Jan 10, 2019

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• Early Identification of Fragile X Syndrome through Expanded Newborn Screening.
  Okoniewski Katherine C et al. Brain sciences 2019 Jan 9(1)
• Clinical Development of Targeted Fragile X Syndrome Treatments: An Industry Perspective.
  Lee Anna W et al. Brain sciences 2018 Dec 8(12)
• A Single Common Assay for Robust and Rapid Fragile X Mental Retardation Syndrome Screening From Dried Blood Spots.
  Tan Vivienne J et al. Frontiers in genetics 2018 9582
• [Fragile X syndrome: new therapeutic strategies].
  Zeidler S et al. Tijdschrift voor psychiatrie 60(5) 338-342
• Challenges in prenatal screening and counselling for fragile X syndrome.
  Mak A Sl et al. Hong Kong medical journal = Xianggang yi xue za zhi 2017 23(2) 108-9
• Diagnostic approach with genetic tests for global developmental delay and/or intellectual disability: Single tertiary center experience.
  Han Ji Yoon et al. Annals of human genetics 2018 Nov
• Fragile X population carrier screening.
  Metcalfe Sylvia A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 20(9) 1091-1092
• A comparison of family financial and employment impacts of fragile X syndrome, autism spectrum disorders, and intellectual disability.
  Ouyang Lijing et al. Research in developmental disabilities 2014 Jul 35(7) 1518-27
• [Genetic screening and prenatal diagnosis for high risk families of Fragile X syndrome].
  Xi Hui et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 Oct 35(5) 653-656
• Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry.
  Utine Gülen Eda et al. European journal of obstetrics, gynecology, and reproductive biology 2018 Feb 22176-80

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