Lv61
2500 积分 2021-02-23 加入
Late-onset autosomal recessive cerebellar ataxia and neuropathy with a novel splicing mutation in the ATM gene
2小时前
待确认
An exploration in pitfalls in interpreting SDHB immunohistochemistry
1个月前
已完结
Two independent mutations in a family with neurofibromatosis type 1 (NF1)
1个月前
已关闭
Germline p.R181H variant in TP53 in a family exemplifying the genotype-phenotype correlations in Li-Fraumeni syndrome
1个月前
已完结
Best Practice for Clinical Somatic Variant Interpretation and Reporting
2个月前
已完结
Co-occurring EGFR p.E709X Mutation Mediates Primary Resistance to the Third-Generation EGFR-TKIs in EGFR p.G719X-Mutant Patients with Advanced NSCLC
3个月前
已完结
Analysis of patient‐specific NF1 variants leads to functional insights for Ras signaling that can impact personalized medicine
3个月前
已完结
The predictive role of ERBB2 point mutations in metastatic colorectal cancer: A systematic review
3个月前
已完结
The relationship among p53 oligomer formation, structure and transcriptional activity using a comprehensive missense mutation library
3个月前
已完结
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