Autor: |
Udayakumar AM; Cytogenetics Laboratory, Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, P.O. Box 35, Muscat 123, Sultanate of Oman. amuk19@hotmail.com, Pathare AV, Al-Kindi S, Khan H, Rehmen JU, Zia F, Al-Ghazaly A, Nusrut N, Khan MI, Wali YA, Al-Lamki Z, Dennison D, Raeburn JA |
Jazyk: |
angličtina |
Zdroj: |
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Sep; Vol. 177 (2), pp. 89-94. |
DOI: |
10.1016/j.cancergencyto.2007.05.014 |
Abstrakt: |
Chromosome aberrations observed at diagnosis are considered to be the most valuable prognostic factors in acute myeloid leukemia (AML). Some specific aberrations vary in frequency among different geographical areas and ethnic groups. There are only limited studies on the role of such variability in AML patients. Here, we report the results of a cytogenetic study on 63 ethnic Omani patients with de novo AML: 18 children (
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Databáze: |
MEDLINE |
Externí odkaz: |
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