Publication: Secondary Burkitt lymphoma in a retinoblastoma patient with 13q deletion syndrome
| dc.contributor.author | Suradej Hongeng | en_US |
| dc.contributor.author | Surapan Parapakpenjun | en_US |
| dc.contributor.author | Samart Pakakasama | en_US |
| dc.contributor.author | Busaba Rerkamnuaychoke | en_US |
| dc.contributor.author | Ratanaporn Pornkul | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.contributor.other | Faculty of Medicine, Ramathibodi Hospital, Mahidol University | en_US |
| dc.date.accessioned | 2018-08-20T06:52:06Z | |
| dc.date.available | 2018-08-20T06:52:06Z | |
| dc.date.issued | 2006-04-01 | en_US |
| dc.description.abstract | We report a boy with constitutional deletion 13q chromosome associated with dysmorphic features and bilateral retinoblastoma. The patient developed secondary Burkitt lymphoma 5 years after the diagnosis of retinoblastoma at the age of 8 months. He has completed treatment for both malignancies. At present, he is 7 years old and still in remission. © 2005 Wiley-Liss, Inc. | en_US |
| dc.identifier.citation | Pediatric Blood and Cancer. Vol.46, No.4 (2006), 524-526 | en_US |
| dc.identifier.doi | 10.1002/pbc.20372 | en_US |
| dc.identifier.issn | 15455017 | en_US |
| dc.identifier.issn | 15455009 | en_US |
| dc.identifier.other | 2-s2.0-33644677387 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/23053 | |
| dc.rights | Mahidol University | en_US |
| dc.rights.holder | SCOPUS | en_US |
| dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33644677387&origin=inward | en_US |
| dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
| dc.subject | Medicine | en_US |
| dc.title | Secondary Burkitt lymphoma in a retinoblastoma patient with 13q deletion syndrome | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33644677387&origin=inward | en_US |