Yayın: An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3
| dc.contributor.author | Gülbaş, Zafer | |
| dc.contributor.author | Gülçin Günden | |
| dc.contributor.author | Eren Gündüz | |
| dc.contributor.author | Olga Meltem Akay | |
| dc.contributor.author | Abdülvahap Aslan | |
| dc.contributor.author | Hülya Özen | |
| dc.contributor.author | Oğuz Çilingir | |
| dc.contributor.author | Ebru Erzurumluoğlu Gökalp | |
| dc.contributor.author | Sinem Kocagil | |
| dc.contributor.author | Sevilhan Artan | |
| dc.contributor.author | Zafer Gülbaş | |
| dc.contributor.author | Beyhan Durak Aras | |
| dc.contributor.orcid | 0000-0003-0243-784X | |
| dc.contributor.orcid | 0000-0003-1707-1764 | |
| dc.contributor.orcid | 0000-0002-6759-1939 | |
| dc.contributor.orcid | 0000-0003-4144-3732 | |
| dc.contributor.orcid | 0000-0002-5593-4164 | |
| dc.contributor.orcid | 0000-0002-1275-5174 | |
| dc.contributor.orcid | 0000-0003-2595-3919 | |
| dc.contributor.orcid | 0000-0001-7658-6309 | |
| dc.contributor.orcid | 0000-0002-4709-0627 | |
| dc.contributor.orcid | 0000-0003-1881-1912 | |
| dc.date.accessioned | 2025-11-13T11:01:37Z | |
| dc.date.issued | 2021-01-01 | |
| dc.identifier.doi | https://doi.org/10.1159/000520242 | |
| dc.identifier.endpage | 487 | |
| dc.identifier.issn | 1424-859X | |
| dc.identifier.issue | 10-11 | |
| dc.identifier.openalex | W4200028922 | |
| dc.identifier.startpage | 479 | |
| dc.identifier.uri | https://hdl.handle.net/11421/5988 | |
| dc.identifier.uri | https://doi.org/10.1159/000520242 | |
| dc.identifier.volume | 161 | |
| dc.language.iso | en | |
| dc.relation.ispartof | Cytogenetic and Genome Research | |
| dc.rights | restrictedAccess | |
| dc.subject | Biology | |
| dc.subject | Loss of heterozygosity | |
| dc.subject | SNP | |
| dc.subject | SNP array | |
| dc.subject | Chronic lymphocytic leukemia | |
| dc.subject | Single-nucleotide polymorphism | |
| dc.subject | Internal medicine | |
| dc.subject | Oncology | |
| dc.subject | Genetics | |
| dc.subject | Leukemia | |
| dc.subject | Gene | |
| dc.subject | Medicine | |
| dc.subject | Genotype | |
| dc.subject | Allele | |
| dc.subject.sdg | 14 | |
| dc.title | An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3 | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.authorid.openalex | A5058571002 |
