File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/S0165-4608(00)00271-5
- Scopus: eid_2-s2.0-0034305149
- PMID: 11104030
- WOS: WOS:000165287100007
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Deletion of Xq23 is a recurrent karyotypic abnormality in acute myeloid leukemia
Title | Deletion of Xq23 is a recurrent karyotypic abnormality in acute myeloid leukemia |
---|---|
Authors | |
Issue Date | 2000 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene |
Citation | Cancer Genetics And Cytogenetics, 2000, v. 122 n. 1, p. 33-36 How to Cite? |
Abstract | Deletion of chromosome Xq23 has been reported in a number of solid tumors, including soft tissue sarcoma, malignant melanoma, astrocytoma, and adenocarcinoma. The deleted Xq often occurs in a setting of very complex karyotypic changes. A similar abnormality has also been described in rare cases of acute myeloid leukemia (AML) but in no other hematologic malignancies. In this study, we report the occurrence of del(X)(q23) in two cases of AML. Copyright (C) 2000 Elsevier Science Inc. |
Persistent Identifier | http://hdl.handle.net/10722/148210 |
ISSN | 2012 Impact Factor: 1.929 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wong, KF | en_US |
dc.contributor.author | Siu, LLP | en_US |
dc.contributor.author | So, CC | en_US |
dc.date.accessioned | 2012-05-29T06:11:31Z | - |
dc.date.available | 2012-05-29T06:11:31Z | - |
dc.date.issued | 2000 | en_US |
dc.identifier.citation | Cancer Genetics And Cytogenetics, 2000, v. 122 n. 1, p. 33-36 | en_US |
dc.identifier.issn | 0165-4608 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/148210 | - |
dc.description.abstract | Deletion of chromosome Xq23 has been reported in a number of solid tumors, including soft tissue sarcoma, malignant melanoma, astrocytoma, and adenocarcinoma. The deleted Xq often occurs in a setting of very complex karyotypic changes. A similar abnormality has also been described in rare cases of acute myeloid leukemia (AML) but in no other hematologic malignancies. In this study, we report the occurrence of del(X)(q23) in two cases of AML. Copyright (C) 2000 Elsevier Science Inc. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene | en_US |
dc.relation.ispartof | Cancer Genetics and Cytogenetics | en_US |
dc.subject.mesh | Acute Disease | en_US |
dc.subject.mesh | Chromosome Deletion | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | In Situ Hybridization, Fluorescence | en_US |
dc.subject.mesh | Karyotyping | en_US |
dc.subject.mesh | Leukemia, Myeloid - Genetics | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | X Chromosome | en_US |
dc.title | Deletion of Xq23 is a recurrent karyotypic abnormality in acute myeloid leukemia | en_US |
dc.type | Article | en_US |
dc.identifier.email | So, CC:scc@pathology.hku.hk | en_US |
dc.identifier.authority | So, CC=rp00391 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/S0165-4608(00)00271-5 | en_US |
dc.identifier.pmid | 11104030 | - |
dc.identifier.scopus | eid_2-s2.0-0034305149 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034305149&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 122 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 33 | en_US |
dc.identifier.epage | 36 | en_US |
dc.identifier.isi | WOS:000165287100007 | - |
dc.publisher.place | United States | en_US |
dc.identifier.issnl | 0165-4608 | - |