Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge

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From 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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• Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge.  
  Lynch Henry T et al. Familial cancer 2017 Oct
• Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.  
  Ripperger Tim et al. American journal of medical genetics. Part A 2017 Apr 173(4) 1017-1037
• Prenatal genetic testing: an investigation of determining factors affecting the decision-making process.  
  Pivetti Monica et al. Journal of genetic counseling 2013 Feb 22(1) 76-89
• Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals.  
  Dheensa Sandi et al. Journal of genetic counseling 2017 Nov
• Ethical issues with newborn screening in the genomics era.  
  Tarini Beth A et al. Annual review of genomics and human genetics 2012 13381-93

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