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Title : Rare Disease Day 2018
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Rare Disease Day 2018

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From Genomics & Health Impact Scan Database

This database includes published scientific literature on evidence-based translation of genomic discoveries into improved health care and disease prevention that have a potential impact on population health.

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• When Celebrities Suddenly Care About Rare Diseases,  
  by Ricki Lewis, PLoS Blogs, June 18
• New consent requirements for newborn screening raise concerns.  
  Yan Wudan et al. Nat. Med. 2015 Jun 4. 21(6) 542-3
• Neurogenetics in Peru: clinical, scientific and ethical perspectives.  
  Cornejo-Olivas Mario et al. J Community Genet 2015 May 27.
• Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm.  
  Larrandaburu Mariela et al. J Community Genet 2015 May 29.
• Rare disease diagnosis: "Rise of the machines",  
  CVID, Primary Immune and Rare Diseases Blog, Apr 1

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