Application of Whole Exome and Targeted Panel Sequencing in the Clinical Molecular Diagnosis of 319 Chinese Families with Inherited Retinal Dystrophy and Comparison Study

類似資料

• Novel mutations of CRB1 in Chinese families presenting with retinal dystrophies
  著者:: Yang, Liping, 等
  出版事項: (2014)
• Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families
  著者:: Yang, Liping, 等
  出版事項: (2013)
• Application of targeted panel sequencing and whole exome sequencing for 76 Chinese families with retinitis pigmentosa
  著者:: Handong Dan, 等
  出版事項: (2020-03-01)
• Application of targeted panel sequencing and whole exome sequencing for 76 Chinese families with retinitis pigmentosa
  著者:: Dan, Handong, 等
  出版事項: (2020)
• Whole exome sequencing using Ion Proton system enables reliable genetic diagnosis of inherited retinal dystrophies
  著者:: Riera, Marina, 等
  出版事項: (2017)