Article: Clinical phenotype of haemoglobin Q-H disease

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TitleClinical phenotype of haemoglobin Q-H disease
AuthorsLeung, KFS1
Ma, ESK1
Chan, AYY1
Chan, LC1
Issue Date2004
PublisherB M J Publishing Group. The Journal's web site is located at http://jcp.bmjjournals.com/
CitationJournal Of Clinical Pathology, 2004, v. 57 n. 1, p. 81-82 [How to Cite?]
DOI: http://dx.doi.org/10.1136/jcp.57.1.81
AbstractSeven patients of Chinese origin who had haemoglobin (Hb) Q-H disease were studied. They were found to have a similar clinical phenotype to that of patients with deletional Hb H disease, who have a near identical genotypic configuration. The complete absence of Hb A in Hb Q-H disease and the similar clinical phenotype to deletional Hb H disease lends support to the observation that Hb Q-Thailand shares similar functional properties with Hb A.
ISSN0021-9746
2011 Impact Factor: 2.306
2011 SCImago Journal Rankings: 0.236
DOIhttp://dx.doi.org/10.1136/jcp.57.1.81
ISI Accession Number IDWOS:000187535900018
PubMed Central IDPMC1770185
ReferencesReferences in Scopus
DC Field
Value
dc.contributor.authorLeung, KFS
dc.contributor.authorMa, ESK
dc.contributor.authorChan, AYY
dc.contributor.authorChan, LC
dc.date.accessioned2007-03-23T04:50:20Z
dc.date.available2007-03-23T04:50:20Z
dc.date.issued2004
dc.description.abstractSeven patients of Chinese origin who had haemoglobin (Hb) Q-H disease were studied. They were found to have a similar clinical phenotype to that of patients with deletional Hb H disease, who have a near identical genotypic configuration. The complete absence of Hb A in Hb Q-H disease and the similar clinical phenotype to deletional Hb H disease lends support to the observation that Hb Q-Thailand shares similar functional properties with Hb A.
dc.description.naturepublished_or_final_version
dc.format.extent203347 bytes
dc.format.extent26624 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypeapplication/msword
dc.identifier.citationJournal Of Clinical Pathology, 2004, v. 57 n. 1, p. 81-82 [How to Cite?]
DOI: http://dx.doi.org/10.1136/jcp.57.1.81
dc.identifier.doihttp://dx.doi.org/10.1136/jcp.57.1.81
dc.identifier.epage82
dc.identifier.hkuros86077
dc.identifier.isiWOS:000187535900018
dc.identifier.issn0021-9746
2011 Impact Factor: 2.306
2011 SCImago Journal Rankings: 0.236
dc.identifier.issue1
dc.identifier.openurl
dc.identifier.pmcidPMC1770185
dc.identifier.pmid14693843
dc.identifier.scopuseid_2-s2.0-0345863811
dc.identifier.spage81
dc.identifier.urihttp://hdl.handle.net/10722/43613
dc.identifier.volume57
dc.languageeng
dc.publisherB M J Publishing Group. The Journal's web site is located at http://jcp.bmjjournals.com/
dc.publisher.placeUnited Kingdom
dc.relation.ispartofJournal of Clinical Pathology
dc.relation.referencesReferences in Scopus
dc.rightsJournal of Clinical Pathology. Copyright © B M J Publishing Group.
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License
dc.subject.meshHemoglobin h - analysis
dc.subject.meshHemoglobins, abnormal - analysis
dc.subject.meshThalassemia - blood
dc.subject.meshPhenotype
dc.subject.meshHemoglobin a - analysis
dc.titleClinical phenotype of haemoglobin Q-H disease
dc.typeArticle
Author Affiliations
  1. The University of Hong Kong