File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: An unbalanced translocation, der(17)t(1;17)(p13;p11.2), leads to heterozygous loss of TP53 and is associated with clinical evolution in myelodysplastic syndrome

TitleAn unbalanced translocation, der(17)t(1;17)(p13;p11.2), leads to heterozygous loss of TP53 and is associated with clinical evolution in myelodysplastic syndrome
Authors
Issue Date2008
PublisherStep Communications Ltd. The Journal's web site is located at http://www.ibms.org/index.cfm?method=publications.british_journal
Citation
British Journal Of Biomedical Science, 2008, v. 65 n. 1, p. 36-38 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/148552
ISSN
2015 Impact Factor: 1.245
2015 SCImago Journal Rankings: 0.352
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorSo, CCen_US
dc.contributor.authorWan, TSKen_US
dc.contributor.authorMa, ESKen_US
dc.contributor.authorChan, LCen_US
dc.date.accessioned2012-05-29T06:13:41Z-
dc.date.available2012-05-29T06:13:41Z-
dc.date.issued2008en_US
dc.identifier.citationBritish Journal Of Biomedical Science, 2008, v. 65 n. 1, p. 36-38en_US
dc.identifier.issn0967-4845en_US
dc.identifier.urihttp://hdl.handle.net/10722/148552-
dc.languageengen_US
dc.publisherStep Communications Ltd. The Journal's web site is located at http://www.ibms.org/index.cfm?method=publications.british_journalen_US
dc.relation.ispartofBritish Journal of Biomedical Scienceen_US
dc.subject.meshAgeden_US
dc.subject.meshAnemia - Genetics - Physiopathologyen_US
dc.subject.meshCytogenetic Analysis - Methodsen_US
dc.subject.meshDisease Progressionen_US
dc.subject.meshFemaleen_US
dc.subject.meshGene Deletionen_US
dc.subject.meshGenes, P53en_US
dc.subject.meshHumansen_US
dc.subject.meshMyelodysplastic Syndromes - Diagnosis - Geneticsen_US
dc.subject.meshTranslocation, Geneticen_US
dc.titleAn unbalanced translocation, der(17)t(1;17)(p13;p11.2), leads to heterozygous loss of TP53 and is associated with clinical evolution in myelodysplastic syndromeen_US
dc.typeArticleen_US
dc.identifier.emailSo, CC:scc@pathology.hku.hken_US
dc.identifier.emailChan, LC:chanlc@hkucc.hku.hken_US
dc.identifier.authoritySo, CC=rp00391en_US
dc.identifier.authorityChan, LC=rp00373en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.pmid18476495-
dc.identifier.scopuseid_2-s2.0-41749119162en_US
dc.identifier.hkuros150511en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-41749119162&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume65en_US
dc.identifier.issue1en_US
dc.identifier.spage36en_US
dc.identifier.epage38en_US
dc.identifier.isiWOS:000254599200009-
dc.publisher.placeUnited Kingdomen_US

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats