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

Παρόμοια τεκμήρια

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