Associated Papers
A novel stop codon mutation in STK11 gene is associated with Peutz-Jeghers Syndrome and elevated cancer risk: a case study.
Khanabadi B et al.
Gastroenterology and Hepatology From Bed to Bench, 2023
Clinical Practice of Targeted Capture Sequencing to Identify Actionable Alterations in Cholangiocarcinoma.
Ma K et al.
Cancers, 2022
36291846 (PubMed )
Supplement: cancers-14-05062-s001.zip › Supplementary_Tables.xlsx › Table_S3
STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients.
Jiang YL et al.
Cancer Genetics, 2019
The impact of the Cancer Genome Atlas on lung cancer.
Chang JT et al.
Translational Research : the Journal of Laboratory and Clinical Medicine, 2015
Genetic and Clinical Analyses of Southern Chinese Children with Peutz-Jeghers Syndrome.
Fu J et al.
Genetic Testing and Molecular Biomarkers, 2015
RADIA: RNA and DNA integrated analysis for somatic mutation detection.
Radenbaugh AJ et al.
Plos One, 2014
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.
Hearle N et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2006
Select a paper to view details