Whole exome sequencing in fetal cardiac rhabdomyoma detected by ultrasonography: an analysis of 12 cases
Abstract Background Most of fetal cardiac rhabdomyomas (CRs) are associated with tuberous sclerosis (TSC), an autosomal dominant inherited disorder caused by mutations in the TSC1 or TSC2 genes. Methods In this study, 12 fetuses with sonographically identified CR were included. A comprehensive analy...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BMC
2025-11-01
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| Cyfres: | BMC Pregnancy and Childbirth |
| Pynciau: | |
| Mynediad Ar-lein: | https://doi.org/10.1186/s12884-025-08365-7 |
| Tagiau: |
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