Publication:
Hairy cell leukemia in father and son

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dc.contributor.authorsCetiner, M; Adiguzel, C; Argon, D; Ratip, S; Eksioglu-Demiralp, E; Tecimer, T; Bayik, M
dc.date.accessioned2022-03-10T11:19:44Z
dc.date.accessioned2026-01-10T17:00:10Z
dc.date.available2022-03-10T11:19:44Z
dc.date.issued2003
dc.description.abstractHairy cell leukemia (HCL) is an uncommon B cell disorder, and familial HCL is rarely encountered among the first degree relatives of HCL patients. A father and son, both of whom developed hairy cell leukemia, is presented in this report. The HLA haplotype shared by the father and son was A2, B18, BW6, CW7, DR3, DR10, and DQ8. Among these haplotypes, HLA A2 and Bw6 have previously been reported.
dc.identifier.doi10.1385/MO:20:4:375
dc.identifier.issn1357-0560
dc.identifier.pubmed14716034
dc.identifier.urihttps://hdl.handle.net/11424/219542
dc.identifier.wosWOS:000187156000008
dc.language.isoeng
dc.publisherHUMANA PRESS INC
dc.relation.ispartofMEDICAL ONCOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectfamilial hairy cell leukemia.
dc.subjectHLA-LINKED DISEASE
dc.subject2 BROTHERS
dc.subjectEPIDEMIOLOGY
dc.subjectSIBLINGS
dc.titleHairy cell leukemia in father and son
dc.typeeditorial
dspace.entity.typePublication
oaire.citation.endPage378
oaire.citation.issue4
oaire.citation.startPage375
oaire.citation.titleMEDICAL ONCOLOGY
oaire.citation.volume20

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