Lv31
360 积分 2024-09-10 加入
Fragile X Syndrome Carrier Screening Using a Nanopore Sequencing Assay
29天前
已完结
A 12-gene pharmacogenetic panel to prevent adverse drug reactions: an open-label, multicentre, controlled, cluster-randomised crossover implementation study
30天前
已完结
Clinical validation of RNA sequencing for Mendelian disorder diagnostics
1个月前
已完结
Genotypic and phenotypic characteristics of ADGRV1 mutations in four children and functional validation in a zebrafish model
1个月前
已完结
Extrachromosomal DNA maintenance and DNA damage response: A bidirectional axis in cancer progression and therapy
1个月前
已关闭
Single-cell eQTL analysis identifies genetic variation underlying metabolic dysfunction-associated steatohepatitis
1个月前
已完结
RNA splicing dysregulation and the hallmarks of cancer
2个月前
已完结
Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases
2个月前
已完结
Deep learning using histological images for gene mutation prediction in lung cancer: a multicentre retrospective study
2个月前
已完结
Molecular stratification of idiopathic nephrotic syndrome
2个月前
已完结
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