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Article: First-trimester diagnosis of hydrolethalus syndrome in a Chinese family

TitleFirst-trimester diagnosis of hydrolethalus syndrome in a Chinese family
Authors
Issue Date2004
Citation
Prenatal Diagnosis, 2004, v. 24 n. 8, p. 587-590 How to Cite?
AbstractWe report a case resembling hydrolethalus syndrome in a Chinese family. Fetal polydactyly, syndactyly, encephalocele and cardiac malformation were detected on ultrasound examination at 12 weeks' gestation. Termination of pregnancy was performed, and postmortem examination confirmed the findings. This is the first report of a first-trimester prenatal diagnosis of hydrolethalus syndrome in the Chinese population. Copyright © 2004 John Wiley & Sons, Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/194212
ISSN
2015 Impact Factor: 3.043
2015 SCImago Journal Rankings: 1.450
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChan, BCP-
dc.contributor.authorShek, TWH-
dc.contributor.authorLee, CP-
dc.date.accessioned2014-01-30T03:32:18Z-
dc.date.available2014-01-30T03:32:18Z-
dc.date.issued2004-
dc.identifier.citationPrenatal Diagnosis, 2004, v. 24 n. 8, p. 587-590-
dc.identifier.issn0197-3851-
dc.identifier.urihttp://hdl.handle.net/10722/194212-
dc.description.abstractWe report a case resembling hydrolethalus syndrome in a Chinese family. Fetal polydactyly, syndactyly, encephalocele and cardiac malformation were detected on ultrasound examination at 12 weeks' gestation. Termination of pregnancy was performed, and postmortem examination confirmed the findings. This is the first report of a first-trimester prenatal diagnosis of hydrolethalus syndrome in the Chinese population. Copyright © 2004 John Wiley & Sons, Ltd.-
dc.languageeng-
dc.relation.ispartofPrenatal Diagnosis-
dc.titleFirst-trimester diagnosis of hydrolethalus syndrome in a Chinese family-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/pd.870-
dc.identifier.pmid15305343-
dc.identifier.scopuseid_2-s2.0-4243191527-
dc.identifier.volume24-
dc.identifier.issue8-
dc.identifier.spage587-
dc.identifier.epage590-
dc.identifier.isiWOS:000223530300001-

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