Lv2
116 积分 2025-10-23 加入
TaoHeChengQi Decotion alleviate chronic renal failure via regulation of PHD2/UCP1 and RIPK3/AKT/TGF-β pathway
5天前
已完结
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
12天前
已完结
Functionalized Decalcified Bone Matrix Scaffold for Cartilage and Bone Regeneration and Repair of Osteochondral Composite Defects
14天前
已完结
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause
1个月前
已完结
The Role of Splicing Factor SF3B4 in Congenital Diseases and Tumors
1个月前
已关闭
A systematic review on Treacher Collins syndrome: Correlation between molecular genetic findings and clinical severity
1个月前
已完结
Arthrogryposis multiplex congenita: dental and maxillofacial phenotype - A scoping review
1个月前
已完结
Genetic Bases of Arthrogryposis Multiplex Congenita
1个月前
已完结
A Novel Homozygous RRP12 Variant in a Chinese Patient with Early‐Onset Cerebellar Ataxia
1个月前
已完结
Characterization of Novel Splicing Mutations and a Recurrent Deletion in COLQ Congenital Myasthenic Syndrome
1个月前
已完结
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