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Article: Alpha-thalassaemia

TitleAlpha-thalassaemia
Authors
Leung, WCLeung, KYLau, ETTang, MHYChan, V
KeywordsAlpha-thalassaemia
Haemoglobin (Hb) Bart's
Pre-implantation genetic diagnosis
Prenatal diagnosis
Screening
Issue Date2008
PublisherElsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/siny
Citation
Seminars In Fetal And Neonatal Medicine, 2008, v. 13 n. 4, p. 215-222 How to Cite?
DOI: http://dx.doi.org/10.1016/j.siny.2008.02.006
AbstractAlpha-thalassaemia is one of the most common human genetic disorders. Couples in which both partners carry alpha 0-thalassaemia traits have a 25% risk of having a fetus affected by homozygous alpha-thalassaemia or haemoglobin Bart's disease, with severe fetal anaemia in utero, hydrops fetalis, stillbirth or early neonatal death, as well as causing various maternal morbidities. This disorder is common in southeast Asia and southern China, and the expanding populations of southeast Asian immigrants in the US, Canada, UK and Europe mean that this disorder is no longer rare in these countries. © 2008 Elsevier Ltd. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/59139
ISSN
1744-165X
2021 Impact Factor: 3.726
2020 SCImago Journal Rankings: 1.404
ISI Accession Number ID
WOS:000257609400003
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorLeung, WCen_HK
dc.contributor.authorLeung, KYen_HK
dc.contributor.authorLau, ETen_HK
dc.contributor.authorTang, MHYen_HK
dc.contributor.authorChan, Ven_HK
dc.date.accessioned2010-05-31T03:43:38Z-
dc.date.available2010-05-31T03:43:38Z-
dc.date.issued2008en_HK
dc.identifier.citationSeminars In Fetal And Neonatal Medicine, 2008, v. 13 n. 4, p. 215-222en_HK
dc.identifier.issn1744-165Xen_HK
dc.identifier.urihttp://hdl.handle.net/10722/59139-
dc.description.abstractAlpha-thalassaemia is one of the most common human genetic disorders. Couples in which both partners carry alpha 0-thalassaemia traits have a 25% risk of having a fetus affected by homozygous alpha-thalassaemia or haemoglobin Bart's disease, with severe fetal anaemia in utero, hydrops fetalis, stillbirth or early neonatal death, as well as causing various maternal morbidities. This disorder is common in southeast Asia and southern China, and the expanding populations of southeast Asian immigrants in the US, Canada, UK and Europe mean that this disorder is no longer rare in these countries. © 2008 Elsevier Ltd. All rights reserved.en_HK
dc.languageengen_HK
dc.publisherElsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/sinyen_HK
dc.relation.ispartofSeminars in Fetal and Neonatal Medicineen_HK
dc.subjectAlpha-thalassaemiaen_HK
dc.subjectHaemoglobin (Hb) Bart'sen_HK
dc.subjectPre-implantation genetic diagnosisen_HK
dc.subjectPrenatal diagnosisen_HK
dc.subjectScreeningen_HK
dc.subject.meshFemaleen_HK
dc.subject.meshHumansen_HK
dc.subject.meshMass Screeningen_HK
dc.subject.meshPregnancyen_HK
dc.subject.meshPreimplantation Diagnosisen_HK
dc.subject.meshPrenatal Diagnosisen_HK
dc.subject.meshalpha-Thalassemia - diagnosis - geneticsen_HK
dc.titleAlpha-thalassaemiaen_HK
dc.typeArticleen_HK
dc.identifier.emailTang, MHY: mhytang@hkucc.hku.hken_HK
dc.identifier.emailChan, V: vnychana@hkucc.hku.hken_HK
dc.identifier.authorityTang, MHY=rp01701en_HK
dc.identifier.authorityChan, V=rp00320en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.siny.2008.02.006en_HK
dc.identifier.pmid18406222-
dc.identifier.scopuseid_2-s2.0-44649172367en_HK
dc.identifier.hkuros149197en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-44649172367&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume13en_HK
dc.identifier.issue4en_HK
dc.identifier.spage215en_HK
dc.identifier.epage222en_HK
dc.identifier.isiWOS:000257609400003-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridLeung, WC=7201504435en_HK
dc.identifier.scopusauthoridLeung, KY=8247106900en_HK
dc.identifier.scopusauthoridLau, ET=36006491400en_HK
dc.identifier.scopusauthoridTang, MHY=35362943900en_HK
dc.identifier.scopusauthoridChan, V=7202654865en_HK
dc.identifier.issnl1744-165X-

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