Associated Papers
Whole exome sequencing identifies novel somatic variants in Xinjiang Kazak esophageal squamous cell carcinoma.
Wang MB et al.
Pathology, Research and Practice, 2025
From musk to body odor: Decoding olfaction through genetic variation.
Li B et al.
Plos Genetics, 2022
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Ogata T et al.
Plos One, 2014
24637876 (PubMed )
Supplement: pone.0091598.s004.pdf
The Clinical Relevance of Frequent Germline Genetic Variants Detected by Targeted Sequencing in Patients With Rectal Adenocarcinoma (READ).
Huang KC et al.
Cancer Genomics & Proteomics, 0
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