Free Access
Med Sci (Paris)
Volume 33, Number 11, Novembre 2017
Page(s) 1001 - 1002
Section Repères
Published online 04 December 2017
  1. Yang Y, Muzny DM, Xia F, et al. Molecular findings among patients referred for clinical whole-exome sequencing. JAMA 2014 ; 312 : 1870–1879. [CrossRef] [PubMed] [Google Scholar]
  2. Clément S, Gargiulo M, Feingold J, Durr A. Guidelines for presymptomatic testing for Huntington’s disease: past, present and future in France. Rev Neurol (Paris) 2015 ; 171 : 572–580. [CrossRef] [PubMed] [Google Scholar]
  3. Godino L, Turchetti D, Jackson L, et al. Impact of presymptomatic genetic testing on young adults: a systematic review. Eur J Hum Genet 2016 ; 24 : 496–503. [CrossRef] [PubMed] [Google Scholar]
  4. Kalia SS, Adelman K, Bale SJ, et al. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of medical genetics and genomics. Genet Med 2017 ; 19 : 249–255. [CrossRef] [PubMed] [Google Scholar]
  5. Chen R, Shi L, Hakenberg J, et al. Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases. Nat Biotechnol 2016 ; 34 : 531–538. [CrossRef] [PubMed] [Google Scholar]

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