Associated Papers
Identification of heritable rare variants associated with early-stage lung adenocarcinoma risk.
Fu R et al.
Translational Lung Cancer Research, 2022
35529798 (PubMed )
Supplement: tlcr-11-04-509-supplementary.pdf
Comprehensive Study of Germline Mutations and Double-Hit Events in Esophageal Squamous Cell Cancer.
Zeng B et al.
Frontiers in Oncology, 2021
33889545 (PubMed )
Supplement: Table_6.xlsx › Sheet1
Nanopore Targeted Sequencing for Rapid Gene Mutations Detection in Acute Myeloid Leukemia.
Cumbo C et al.
Genes, 2019
Contribution of de novo and mosaic TP53 mutations to Li-Fraumeni syndrome.
Renaux-Petel M et al.
Journal of Medical Genetics, 2018
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