Associated Papers
MST1R Gene Variants Predispose Individuals to Tetralogy of Fallot.
Feng Z et al.
Phenomics (cham, Switzerland), 2024
GISTs with NTRK Gene Fusions: A Clinicopathological, Immunophenotypic, and Molecular Study.
Cao Z et al.
Cancers, 2022
36612101 (PubMed )
Supplement: cancers-15-00105-s001.zip › cancers-2037302-supplementary.pdf
A novel 8.57-kb deletion of the upstream region of PRKAR1A in a family with Carney complex.
Ito S et al.
Molecular Genetics & Genomic Medicine, 2022
35128829 (PubMed )
Supplement: MGG3-10-e1884-s003.xlsx › Supplementary_Table_1
Clinical utility of comprehensive genomic profiling in Japan: Result of PROFILE-F study.
Aoyagi Y et al.
Plos One, 2022
35358259 (PubMed )
Supplement: pone.0266112.s001.xlsx › Patients
Comprehensive germline and somatic genomic profiles of Chinese patients with biliary tract cancer.
Yu H et al.
Frontiers in Oncology, 2022
36072793 (PubMed )
Supplement: Table_2.xlsx › germline_alterations
A Gly684Ala substitution in the androgen receptor is the cause for azoospermia in a Chinese family with mild androgen insensitivity syndrome and normal hormone levels.
Yuan Y et al.
Frontiers in Genetics, 2022
36159980 (PubMed )
Supplement: Table1.XLSX › SNP
Identification of Key Genes Mutations Associated With the Radiosensitivity by Whole Exome Sequencing in Pancreatic Cancer.
Hu B et al.
Frontiers in Oncology, 2021
34434896 (PubMed )
Supplement: DataSheet_5.xlsx › All.final.xls.sed
Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinoma.
Dai W et al.
Proceedings of the National Academy of Sciences of the United States of America, 2016
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