Lv4
510 积分 2021-08-03 加入
一例孤独症患儿的全基因组拷贝数变异分析
21小时前
待确认
[Genome-wide copy number microarray analysis for a boy with autism]
21小时前
已关闭
Distal trisomy 14q due to tandem duplication (q24 leads to q32)
2个月前
已关闭
运用光学基因组图谱技术诊断1例复杂染色体结构重排
6个月前
已完结
母源性复杂染色体重排致胎儿染色体结构异常：3例分析
6个月前
已完结
A neonatal case of congenital blastic plasmacytoid dendritic cell neoplasm with KMT2C gene duplication
6个月前
已完结
[Clinical and genetic analysis of three pediatric patients with 15q24 microdeletion syndrome]
7个月前
已关闭
Molecular cytogenetic characterization of isolated recurrent 4q35.2 microduplication in Chinese population: a seven-year single-center retrospective study
8个月前
已关闭
Prospective Investigation of Optical Genome Mapping for Prenatal Genetic Diagnosis
9个月前
已完结
Proximity extension assay proteomics and renal single cell transcriptomics uncover novel urinary biomarkers for active lupus nephritis
10个月前
已完结
皖公网安备34019202002308
