Lv2
180 积分 2023-09-16 加入
Rare mutation-dominant compound EGFR-positive NSCLC is associated with enriched kinase domain-resided variants of uncertain significance and poor clinical outcomes
15小时前
待确认
Phenotypic and clinical manifestations of compound heterozygous genetic haemochromatosis (CHGH): a non‐invasive approach to clinical management
21天前
已完结
A novel compound mutation of SLCO2A1 in a Chinese patient with Primary hypertrophic osteoarthropathy
21天前
已完结
Novel compound variants of the <em>TMTC3</em> gene cause cobblestone lissencephaly‑like syndrome: A case report
27天前
已完结
Molecular genetics of malignant insulinoma
27天前
已关闭
Identification of mutations at DNA topoisomerase I responsible for camptothecin resistance
27天前
已关闭
Autoinflammatory syndromes with coexisting variants in Mediterranean FeVer and other genes: Utility of multiple gene screening and the possible impact of gene dosage
27天前
已完结
Comment on “RAS/TP53 co-Mutation is Associated With Worse Survival After Concurrent Resection of Colorectal Liver Metastases and Extrahepatic Disease”
27天前
已完结
[Hemoglobin Woodville associated with double point mutation in the gene of glucose-6-phosphate dehydrogenase]
27天前
已完结
Hepatocellular adenoma with a double mutation HNF1A and IDH1 in a patient with Ollier disease
27天前
已完结
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