Lv63
2480 积分 2022-03-30 加入
Comparing Baseline VAF in Circulating tumor DNA and Tumor Tissues Predicting Prognosis of Patients with Colorectal Cancer Liver Metastases After Curative Resection
                                            7小时前
                                            已完结
                                        
SDHD Immunohistochemistry: A New Tool to ValidateSDHxMutations in Pheochromocytoma/Paraganglioma
                                            7天前
                                            已完结
                                        
Development of a targeted gene panel for the diagnosis of Gorlin syndrome
                                            13天前
                                            已完结
                                        
SLC4A11 mutations in Fuchs endothelial corneal dystrophy
                                            21天前
                                            已完结
                                        
Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort
                                            28天前
                                            已关闭
                                        
Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort
                                            28天前
                                            已完结
                                        
A case of rare splice-site Bruton's tyrosine kinase mutation with atypical X-linked agammaglobulinemia
                                            1个月前
                                            已完结
                                        
Genetic Architecture of Azoospermia—Time to Advance the Standard of Care
                                            1个月前
                                            已完结
                                        
Probing the biological consequences of a previously undescribed de novo mutation of ZMYND11 in a schizophrenia patient by CRISPR genome editing and induced pluripotent stem cell based in vitro disease-modeling
                                            1个月前
                                            已完结
                                        
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a caucasian kindred
                                            1个月前
                                            已完结