Ethical issues raised by common copy number variants and single nucleotide polymorphisms of certain and uncertain significance in general medical practice

Lignende værker

• Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants
  Udgivet: (2009)
• Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come?
  af: Cheon, Jae Yeon, et al.
  Udgivet: (2014)
• Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?
  af: Rotshenker-Olshinka, Keren, et al.
  Udgivet: (2021)
• Mutations in the recD gene of Escherichia coli that raise the copy number of certain plasmids.
  af: Seelke, R, et al.
  Udgivet: (1987)
• The clinical significance of small copy number variants in neurodevelopmental disorders
  af: Asadollahi, Reza, et al.
  Udgivet: (2014)