Pitfalls in interpretation of CFTR variants in the context of incidental findings. Boussaroque Agathe et al. Human mutation 2019 Jul

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Last Posted: Aug 01, 2019

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• Pitfalls in interpretation of CFTR variants in the context of incidental findings.
  Boussaroque Agathe et al. Human mutation 2019 Jul
• Diagnostic yield of next-generation sequencing applied to neurological disorders.
  Marques Matos Cláudia et al. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2019 Jul
• Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.
  Houdayer F et al. European journal of medical genetics 2019 Jun 103711
• Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas.
  van der Schoot V et al. Human reproduction (Oxford, England) 2019 May
• Points-to-consider on the return of results in epigenetic research.
  Dyke Stephanie O M et al. Genome medicine 2019 May 11(1) 31
• Genomic testing in myeloid malignancy.
  Docking T Roderick et al. International journal of laboratory hematology 2019 May 41 Suppl 1117-125
• Finding Out You Have a Genetic Mutation May Not Be as Bad as You Think- Scientists are learning they greatly overestimated chances of developing deadly cancers in patients with no family history of disease 
  M Cortez, Bloomberg News, May 9, 2019
• Inherited cardiomyopathies.
  Miles Chris et al. BMJ (Clinical research ed.) 2019 05 l1570
• A Tale of Two Capacities: Including Children and Decisionally Vulnerable Adults in Biomedical Research.
  Dalpé Gratien et al. Frontiers in genetics 2019 10289
• The use of ACMG secondary findings recommendations for general population screening: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
  ACMG Board of Directors, Genetics in Medicine, April 25, 2019

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