Lv32
310 积分 2023-10-29 加入
SCS: cell segmentation for high-resolution spatial transcriptomics
5小时前
已完结
3-Methylcrotonyl-CoA carboxylase deficiency: Mutational spectrum derived from comprehensive newborn screening
28天前
已完结
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity ofMCCA andMCCB mutations and impact on risk assessment
28天前
已完结
Alkaptonuria: a rare disease with multiorgan manifestation and a long-awaited diagnosis
28天前
已完结
A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency
28天前
已完结
Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutation
28天前
已完结
Methylcrotonoyl-Coa Carboxylase 2 Overexpression Predicts An Unfavorable Prognosis and Promotes Cell Proliferation in Breast Cancer
28天前
已完结
Methylcrotonoyl-Coa Carboxylase 2 Overexpression Predicts An Unfavorable Prognosis and Promotes Cell Proliferation in Breast Cancer
28天前
已关闭
[Genetic analysis of children with nonsyndromic sensorineural hearing loss due to novel mutations/deletions of
1个月前
已完结
Human Amniotic Membrane: A Versatile Scaffold for Tissue Engineering
1个月前
已完结
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