Associated Papers
Unraveling the genetic causes in large pedigrees with gout by whole‑exome sequencing.
Xia X et al.
International Journal of Molecular Medicine, 2020
Costello syndrome: Clinical phenotype, genotype, and management guidelines.
Gripp KW et al.
American Journal of Medical Genetics. Part A, 2019
RET Aberrations in Diverse Cancers: Next-Generation Sequencing of 4,871 Patients.
Kato S et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2017
27683183 (PubMed )
Supplement: 10780432ccr161679-sup-168576_1_supp_3636667_wcc1ns.docx
Glycoproteomic Approach Identifies KRAS as a Positive Regulator of CREG1 in Non-small Cell Lung Cancer Cells.
Clark DJ et al.
Theranostics, 2016
Somatic changes in primary liver cancer in Russia: a pilot study.
Kalinina O et al.
Mutation Research, 2013
LKB1 mutations frequently detected in mucinous bronchioloalveolar carcinoma.
Osoegawa A et al.
Japanese Journal of Clinical Oncology, 2011
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