P661: A database of high allele frequency variants from exome sequencing data of 20,455 patients enriched with Asian population

Slični predmeti

• P661: A database of high allele frequency variants from exome sequencing data of 20,455 patients enriched with Asian population
  od: Kisang Kwon, i dr.
  Izdano: (2023-01-01)
• Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders
  od: Heonjong Han, i dr.
  Izdano: (2025-01-01)
• Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family
  od: Seung Woo Ryu, i dr.
  Izdano: (2024-03-01)
• P670: A collaborative model integrating clinical genetics and molecular pathology for tumor/normal paired whole exome sequencing testing
  od: Yi Liu, i dr.
  Izdano: (2024-01-01)
• A first large study of whole-exome sequencing (WES) in 489 patients with suspected rare genetic disorders at a tertiary centre in Malaysia
  od: Lip Hen Moey, i dr.
  Izdano: (2025-01-01)