Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants

مواد مشابهة

• Systematic assessment of copy-number variant detection via genome-wide single nucleotide polymorphism genotyping
  بواسطة: Cooper, Gregory M., وآخرون
  منشور في: (2008)
• Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses
  بواسطة: Penney, Michelle E., وآخرون
  منشور في: (2018)
• Ethical issues raised by common copy number variants and single nucleotide polymorphisms of certain and uncertain significance in general medical practice
  بواسطة: Beaudet, Arthur L
  منشور في: (2010)
• A genome-wide single nucleotide polymorphism and copy number variation analysis for number of piglets born alive
  بواسطة: Stafuzza, Nedenia Bonvino, وآخرون
  منشور في: (2019)
• Genetic copy number variants in myocardial infarction patients with hyperlipidemia
  بواسطة: Shia, Wei-Chung, وآخرون
  منشور في: (2011)