Pages that link to "Q54181235"
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The following pages link to Association of TBX20 gene polymorphism with congenital heart disease in Han Chinese neonates. (Q54181235):
Displaying 5 items.
- Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population (Q36754690) (← links)
- Silencing of TBX20 gene expression in rat myocardial and human embryonic kidney cells leads to cell cycle arrest in G2 phase (Q37297481) (← links)
- TBX1 loss-of-function mutation contributes to congenital conotruncal defects (Q46237828) (← links)
- TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy (Q46708501) (← links)
- Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population (Q48685298) (← links)