| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1010200718 |
| P356 | DOI | 10.1038/SJ.LEU.2402435 |
| P698 | PubMed publication ID | 11960348 |
| P50 | author | Anthony H. Goldstone | Q110167848 |
| Louise Harewood | Q57078104 | ||
| P2093 | author name string | K Roberts | |
| I M Franklin | |||
| C J Harrison | |||
| H G Prentice | |||
| C F Bennett | |||
| S M Richards | |||
| M Martineau | |||
| Medical Research Council Adult Leukaemia Working Party | |||
| G R Jalali | |||
| M S Jabber Al-Obaidi | |||
| P2860 | cites work | Probes for hidden hyperdiploidy in acute lymphoblastic leukaemia | Q73363389 |
| Low frequency of TEL/AML1 in adult acute lymphoblastic leukemia | Q73793495 | ||
| Frequent deletion of chromosome 12p12.3 in children with acute lymphoblastic leukaemia | Q73851062 | ||
| The value of interphase fluorescence in situ hybridization for the detection of translocation t(12;21) in childhood acute lymphoblastic leukemia | Q73932404 | ||
| Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias | Q74068223 | ||
| High rate of chromosome abnormalities detected by fluorescence in situ hybridization using BCR and ABL probes in adult acute lymphoblastic leukemia | Q77299366 | ||
| Transcription factors and translocations in lymphoid and myeloid leukemia | Q34173877 | ||
| Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia. | Q38508281 | ||
| t(12;21): a new recurrent translocation in acute lymphoblastic leukemia. | Q38511359 | ||
| Abnormalities of the ETV6 gene occur in the majority of patients with aberrations of the short arm of chromosome 12: a combined PCR and Southern blotting analysis | Q47841840 | ||
| Discordant results indicating monosomy 8 from FISH and trisomy 8 from chromosome analysis in a patient with chronic lymphocytic leukemia | Q53942025 | ||
| TEL-AML1 fusion in acute lymphoblastic leukaemia of adults | Q58455878 | ||
| The genetics of childhood acute lymphoblastic leukaemia | Q58481922 | ||
| Tandem triplication and quadruplication of chromosome 21 in childhood acute lymphoblastic leukemia | Q71864372 | ||
| Low frequency of the TEL/AML1 fusion gene in acute lymphoblastic leukaemia in Spain | Q73231169 | ||
| P4510 | describes a project that uses | fluorescence in situ hybridization | Q1336182 |
| P433 | issue | 4 | |
| P921 | main subject | leukemia | Q29496 |
| P304 | page(s) | 669-674 | |
| P577 | publication date | 2002-04-01 | |
| P1433 | published in | Leukemia | Q6534498 |
| P1476 | title | ETV6/AML1 fusion by FISH in adult acute lymphoblastic leukemia | |
| P478 | volume | 16 |
| Q46832664 | Abnormalities of the der(12)t(12;21) in ETV6-RUNX1 acute lymphoblastic leukemia. |
| Q58481810 | Acute Lymphoblastic Leukemia |
| Q58481753 | Acute lymphoblastic leukaemia |
| Q58481759 | Acute lymphoblastic leukemia |
| Q58481888 | Amplification of AML1 in acute lymphoblastic leukemia is associated with a poor outcome |
| Q35088805 | Amplification of AML1 on a duplicated chromosome 21 in acute lymphoblastic leukemia: a study of 20 cases. |
| Q33632230 | Clinical features and prognostic implications of TCF3-PBX1 and ETV6-RUNX1 in adult acute lymphoblastic leukemia |
| Q44973480 | Clinicopathological characterization of mammary analogue secretory carcinoma of salivary glands. |
| Q38526944 | Cytogenetic Variation of B-Lymphoblastic Leukemia With Intrachromosomal Amplification of Chromosome 21 (iAMP21): A Multi-Institutional Series Review |
| Q37338855 | Cytogenetic findings of patients with acute lymphoblastic leukemia in fars province |
| Q36730385 | Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature |
| Q84713544 | Cytogenetics and molecular genetics of acute lymphoblastic leukemia |
| Q34304230 | Cytogenetics in acute leukemia |
| Q58481864 | Derivative chromosome 9 deletions are a significant feature of childhood Philadelphia chromosome positive acute lymphoblastic leukaemia |
| Q58481866 | ETV6/RUNX1 fusion at diagnosis and relapse: Some prognostic indications |
| Q58481893 | Frequency of ETV6/AML1 fusion in adult acute lymphoblastic leukemia |
| Q55457412 | Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment. |
| Q41906059 | Guidance for fluorescence in situ hybridization testing in hematologic disorders |
| Q50767297 | High incidence and unique features of antigen receptor gene rearrangements in TEL-AML1-positive leukemias |
| Q28185982 | Mechanism, detection and clinical significance of the reciprocal translocation t(12;21)(p12;q22) in the children suffering from acute lymphoblastic leukaemia |
| Q26749177 | New and emerging prognostic and predictive genetic biomarkers in B-cell precursor acute lymphoblastic leukemia |
| Q92839258 | Pathological features of mammary analogue secretory carcinoma of the salivary gland |
| Q35875306 | Plasma cell myeloma and leukemia |
| Q39992854 | Prognostic and therapeutic role of targetable lesions in B-lineage acute lymphoblastic leukemia without recurrent fusion genes |
| Q92276422 | Recent advances in the biology and treatment of B-cell acute lymphoblastic leukemia |
| Q58481897 | Response to Cuneo et al |
| Q47130030 | Secretory carcinoma - impact of translocation and gene fusions on salivary gland tumor |
| Q53135188 | TEL (ETV6)-AML1 (RUNX1) Initiates Self-Renewing Fetal Pro-B Cells in Association with a Transcriptional Program Shared with Embryonic Stem Cells in Mice |
| Q35779743 | The Runx genes: lineage-specific oncogenes and tumor suppressors |
| Q37995811 | The clinical relevance of chromosomal and genomic abnormalities in B-cell precursor acute lymphoblastic leukaemia |
| Q46393939 | The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1. |
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