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Article: Haemoglobin Q-Thailand and hereditary spherocytosis in a chinese family

TitleHaemoglobin Q-Thailand and hereditary spherocytosis in a chinese family
Authors
Issue Date2001
PublisherBlackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CLH
Citation
Clinical And Laboratory Haematology, 2001, v. 23 n. 1, p. 53-55 How to Cite?
AbstractA Chinese family with concurrent hereditary spherocytosis (HS) and haemoglobin (Hb) Q-Thailand is described. The Hb Q-Thailand mutation was found on the remaining α1 globin gene on a chromosome 16 containing the (-α 4.2) deletion. Active haemolysis in members of this family is segregated with the HS phenotype, and the Hb Q-Thailand in the heterozygous state does not seem to show any modulating effect on HS.
Persistent Identifierhttp://hdl.handle.net/10722/148225
ISSN
2008 Impact Factor: 1.304
2015 SCImago Journal Rankings: 0.654
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorLeung, KFSen_US
dc.contributor.authorAu, WYen_US
dc.contributor.authorChan, AYYen_US
dc.contributor.authorChan, LCen_US
dc.contributor.authorWaye, JSen_US
dc.contributor.authorChui, DHKen_US
dc.contributor.authorMa, SKen_US
dc.date.accessioned2012-05-29T06:11:37Z-
dc.date.available2012-05-29T06:11:37Z-
dc.date.issued2001en_US
dc.identifier.citationClinical And Laboratory Haematology, 2001, v. 23 n. 1, p. 53-55en_US
dc.identifier.issn0141-9854en_US
dc.identifier.urihttp://hdl.handle.net/10722/148225-
dc.description.abstractA Chinese family with concurrent hereditary spherocytosis (HS) and haemoglobin (Hb) Q-Thailand is described. The Hb Q-Thailand mutation was found on the remaining α1 globin gene on a chromosome 16 containing the (-α 4.2) deletion. Active haemolysis in members of this family is segregated with the HS phenotype, and the Hb Q-Thailand in the heterozygous state does not seem to show any modulating effect on HS.en_US
dc.languageengen_US
dc.publisherBlackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CLHen_US
dc.relation.ispartofClinical and Laboratory Haematologyen_US
dc.subject.meshAdulten_US
dc.subject.meshAnemia, Hemolytic, Congenital - Etiology - Geneticsen_US
dc.subject.meshChinaen_US
dc.subject.meshFamily Healthen_US
dc.subject.meshFemaleen_US
dc.subject.meshGenotypeen_US
dc.subject.meshHemoglobins, Abnormal - Geneticsen_US
dc.subject.meshHeterozygoteen_US
dc.subject.meshHumansen_US
dc.subject.meshNuclear Familyen_US
dc.subject.meshOsmotic Fragility - Geneticsen_US
dc.subject.meshPedigreeen_US
dc.subject.meshPhenotypeen_US
dc.subject.meshSpherocytosis, Hereditary - Blood - Complications - Geneticsen_US
dc.titleHaemoglobin Q-Thailand and hereditary spherocytosis in a chinese familyen_US
dc.typeArticleen_US
dc.identifier.emailChan, LC:chanlc@hkucc.hku.hken_US
dc.identifier.authorityChan, LC=rp00373en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1046/j.1365-2257.2001.00349.xen_US
dc.identifier.pmid11422231-
dc.identifier.scopuseid_2-s2.0-0034949481en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0034949481&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume23en_US
dc.identifier.issue1en_US
dc.identifier.spage53en_US
dc.identifier.epage55en_US
dc.identifier.isiWOS:000169881600009-
dc.publisher.placeUnited Kingdomen_US

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