CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

Podobne zapisy

• CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels
  od: Yuan, Bo, i wsp.
  Wydane: (2020)
• An integrated Asian human SNV and indel benchmark established using multiple sequencing methods
  od: Huang, Chuanfeng, i wsp.
  Wydane: (2020)
• Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases
  od: Dharmadhikari, Avinash V., i wsp.
  Wydane: (2019)
• Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases
  od: Avinash V. Dharmadhikari, i wsp.
  Wydane: (2019)
• The dynamic landscape of BRCA1 reversion mutations from indel to SNV in a patient with ovarian cancer treated with PARP-inhibitors and immunotherapy
  od: Jacob, Saya L., i wsp.
  Wydane: (2020)