Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

פריטים דומים

• Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene
  מאת: Rotunno, Melissa, et al.
  יצא לאור: (2016)
• Combined somatic mutation and copy number analysis in the survival of familial CLL
  מאת: Zhou, Weiyin, et al.
  יצא לאור: (2018)
• Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility
  מאת: Yepes, Sally, et al.
  יצא לאור: (2020)
• Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family
  מאת: Pathak, Anand, et al.
  יצא לאור: (2016)
• Common Genetic Variants in Candidate Genes and Risk of Familial Lymphoid Malignancies
  מאת: Liang, Xueying (Sharon), et al.
  יצא לאור: (2009)