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Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing
BACKGROUND: Conotruncal heart defects (CTDs) are heterogeneous congenital heart malformations that result from outflow tract dysplasia; however, the genetic determinants underlying CTDs remain unclear. Increasing evidence demonstrates that dysfunctional TBX2 and TBX3 result in outflow tract malforma...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Hum Genomics |
|---|---|
| Prif Awduron: | , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BioMed Central
2018
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6142335/ https://ncbi.nlm.nih.gov/pubmed/30223900 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-018-0176-0 |
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