Whole exome sequencing and whole genome sequencing improves genetic diagnosis of fetals with heterotaxy syndrome revealed by prenatal ultrasound

2 September 2019 (14:00 - 18:00)
Organised by:
Congress Presentation Part of: Poster Session 5 - Congenital heart disease - Neonatal and pediatric issues Pathophysiology and Mechanisms ESC Premium Access ESC Congress 2019

About the speaker

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Beijing AnZhen Hospital affiliated to Capital Medical University, Beijing (China)

8 More presentations in this session

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Associate Professor L. Eun (Seoul, KR)
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Doctor M. Solari (Grosseto, IT)
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Miss A. Ferreira (Porto, PT)
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Ms S. Dannesbo (Copenhagen, DK)
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Miss E. Blixenkrone-Moeller (Herlev, DK)

The Event

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ESC Congress 2019

2 September 2019 14:00 CET

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