Lv1
60 积分 2024-08-18 加入
Identification and functional validation of variants in the promoter region of HAND1 gene in sporadic tetralogy of Fallot
9小时前
求助中
Individual and joint effects of genetic polymorphisms in microRNA-machinery genes on congenital heart disease susceptibility
11天前
已关闭
NOTCH1 loss of the TAD and PEST domain: An antimorph?
11天前
已完结
From genes to therapy: A comprehensive exploration of congenital heart disease through the lens of genetics and emerging technologies
2个月前
已完结
Gene expression and transcriptional regulation driven by transcription factors involved in congenital heart defects
4个月前
已完结
Functional characterization of GATA6 genetic variants associated with mild congenital heart defects
4个月前
已完结
Jacobsen syndrome: Advances in our knowledge of phenotype and genotype
4个月前
已完结
Congenital heart defects in the recurrent 2q13 deletion syndrome
4个月前
已完结
Expanding the Phenotype of 8p23.1 Deletion Syndrome: Eight New Cases Resembling the Clinical Spectrum of 22q11.2 Microdeletion
4个月前
已完结
Copy-number variation in congenital heart disease
4个月前
已完结
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