File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations

TitleAn Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations
Authors
Lee, HLHMak, ASLKou, KOTPoon, CFWong, WSChiu, KHAu, HHLChan, YKKan, SYATang, MHYLeung, KY
KeywordsCongenital dyserythropoietic anemia
fetal anemia
hydrops fetalis
intrauterine transfusion
Krüppel-like factor 1 (KLF1) gene mutations
Issue Date2016
PublisherInforma Healthcare. The Journal's web site is located at http://informahealthcare.com/loi/hem
Citation
Hemoglobin, 2016, v. 40 n. 6, p. 431-434 How to Cite?
DOI: http://dx.doi.org/10.1080/03630269.2016.1267017
Persistent Identifierhttp://hdl.handle.net/10722/245433
ISSN
0363-0269
2021 Impact Factor: 0.822
2020 SCImago Journal Rankings: 0.300
ISI Accession Number ID
WOS:000398385400015

 

DC FieldValueLanguage
dc.contributor.authorLee, HLH-
dc.contributor.authorMak, ASL-
dc.contributor.authorKou, KOT-
dc.contributor.authorPoon, CF-
dc.contributor.authorWong, WS-
dc.contributor.authorChiu, KH-
dc.contributor.authorAu, HHL-
dc.contributor.authorChan, YK-
dc.contributor.authorKan, SYA-
dc.contributor.authorTang, MHY-
dc.contributor.authorLeung, KY-
dc.date.accessioned2017-09-18T02:10:40Z-
dc.date.available2017-09-18T02:10:40Z-
dc.date.issued2016-
dc.identifier.citationHemoglobin, 2016, v. 40 n. 6, p. 431-434-
dc.identifier.issn0363-0269-
dc.identifier.urihttp://hdl.handle.net/10722/245433-
dc.languageeng-
dc.publisherInforma Healthcare. The Journal's web site is located at http://informahealthcare.com/loi/hem-
dc.relation.ispartofHemoglobin-
dc.rightsHemoglobin. Copyright © Informa Healthcare.-
dc.subjectCongenital dyserythropoietic anemia-
dc.subjectfetal anemia-
dc.subjecthydrops fetalis-
dc.subjectintrauterine transfusion-
dc.subjectKrüppel-like factor 1 (KLF1) gene mutations-
dc.titleAn Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations-
dc.typeArticle-
dc.identifier.emailLee, HLH: lhl102@HKUCC-COM.hku.hk-
dc.identifier.emailChan, YK: ykchanc@hku.hk-
dc.identifier.emailKan, SYA: kansya@hkucc.hku.hk-
dc.identifier.emailTang, MHY: mhytang@hkucc.hku.hk-
dc.identifier.emailLeung, KY: leungkyb@hkucc.hku.hk-
dc.identifier.authorityChan, YK=rp00453-
dc.identifier.authorityTang, MHY=rp01701-
dc.identifier.doi10.1080/03630269.2016.1267017-
dc.identifier.pmid28361594-
dc.identifier.scopuseid_2-s2.0-85016546314-
dc.identifier.hkuros278788-
dc.identifier.volume40-
dc.identifier.issue6-
dc.identifier.spage431-
dc.identifier.epage434-
dc.identifier.isiWOS:000398385400015-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0363-0269-

Export via OAI-PMH Interface in XML Formats

OR

Export to Other Non-XML Formats