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Conference Paper: Identifying the genetic causes underlying prenatally-diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)

TitleIdentifying the genetic causes underlying prenatally-diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)
Authors
Chung, BHY
Issue Date2019
Citation
Health Research Symposium 2019: Genomics and Big Data in Health and Disease, Hong Kong, 12 June 2019 How to Cite?
DescriptionParallel Session 3 – Advanced Medical Research - no. S11
Organizer: Food and Health Bureau (FHB), HKSAR
Persistent Identifierhttp://hdl.handle.net/10722/272445

 

DC FieldValueLanguage
dc.contributor.authorChung, BHY-
dc.date.accessioned2019-07-20T10:42:26Z-
dc.date.available2019-07-20T10:42:26Z-
dc.date.issued2019-
dc.identifier.citationHealth Research Symposium 2019: Genomics and Big Data in Health and Disease, Hong Kong, 12 June 2019-
dc.identifier.urihttp://hdl.handle.net/10722/272445-
dc.descriptionParallel Session 3 – Advanced Medical Research - no. S11-
dc.descriptionOrganizer: Food and Health Bureau (FHB), HKSAR-
dc.languageeng-
dc.relation.ispartofHealth Research Symposium, 2019-
dc.titleIdentifying the genetic causes underlying prenatally-diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)-
dc.typeConference_Paper-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.hkuros298766-

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