Lv11
60 积分 2023-03-20 加入
Splicing defect and functional characterization of the ETFDH c.1049G > A VUS underlying transient MADD: an iPSC and minigene study
2小时前
已完结
Hi-C technology for detection of chromosomal rearrangements in families with adverse pregnancy outcomes: a preliminary exploratory study
2小时前
已完结
Metabolic subtypes and biomarkers in preterm and term neonates via targeted screening
2小时前
求助中
[Analysis of pathogenicity and genotype-phenotype correlation of the c.158G>A variant of phenylalanine hydroxylase gene]
9个月前
已完结
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