Pages that link to "Q34000038"
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The following pages link to Identification of a Novel ZIC3 Isoform and Mutation Screening in Patients with Heterotaxy and Congenital Heart Disease (Q34000038):
Displaying 10 items.
- The ZIC gene family encodes multi-functional proteins essential for patterning and morphogenesis (Q30427638) (← links)
- The determination factors of left-right asymmetry disorders- a short review (Q33693300) (← links)
- Heterotaxy-spectrum heart defects in Zic3 hypomorphic mice (Q34252634) (← links)
- New Genetic Insights into Congenital Heart Disease (Q36106143) (← links)
- Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association (Q36275704) (← links)
- Genetic and functional analyses of ZIC3 variants in congenital heart disease (Q37624304) (← links)
- Transcription factor pathways and congenital heart disease. (Q37997218) (← links)
- Rare novel variants in the ZIC3 gene cause X-linked heterotaxy (Q39608817) (← links)
- Racial disparities in heterotaxy syndrome (Q40581375) (← links)
- Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association (Q90669133) (← links)