Whole-Exome Sequencing for the Discovery of Rare Genetic Variants That Protect from Coronary Artery Disease

Antzeko izenburuak

• Whole‐exome sequencing for variant discovery in blepharospasm
  nork: Tian, Jun, et al.
  Argitaratua: (2018)
• Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
  nork: Raghavan, Neha S., et al.
  Argitaratua: (2018)
• Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
  Argitaratua: (2019)
• Identification of rare genetic variants in Juvenile Idiopathic Arthritis using whole exome sequencing
  nork: Sanchez, E, et al.
  Argitaratua: (2015)
• The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants
  nork: Theisen, J. Graham, et al.
  Argitaratua: (2019)