Lv41
640 积分 2024-09-26 加入
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy
12天前
已完结
Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations
12天前
已完结
Clinical and genetic features of Calpainopathies in Saudi Arabia - a descriptive cross-sectional study
19天前
已完结
Application of machine learning for high-throughput tumor marker screening
1个月前
已完结
Multimodal Analysis of ctDNA Methylation and Fragmentomic Profiles Enhances Detection of Nonmetastatic Colorectal Cancer
1个月前
已完结
Circulating cell-free DNA-based multi-cancer early detection
1个月前
已完结
Saturation genome editing-based clinical classification of BRCA2 variants
2个月前
已完结
[Clinical characteristics and genetic analysis of two children with X-linked Centronuclear myopathy due to variants of MTM1 gene]
3个月前
已关闭
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency
3个月前
已关闭
Clinical and genetic features of sitosterolemia in Japan
3个月前
已完结
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