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Article: Clinical phenotype of haemoglobin Q-H disease
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TitleClinical phenotype of haemoglobin Q-H disease
 
AuthorsLeung, KFS1
Ma, ESK1 1
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
2012 Impact Factor: 2.439
2012 SCImago Journal Rankings: 0.980
 
DOIhttp://dx.doi.org/10.1136/jcp.57.1.81
 
PubMed Central IDPMC1770185
 
ISI Accession Number IDWOS:000187535900018
 
ReferencesReferences in Scopus
 
DC FieldValue
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
2012 Impact Factor: 2.439
2012 SCImago Journal Rankings: 0.980
 
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
 
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Author Affiliations
  1. The University of Hong Kong