| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0959-8049(98)00433-X |
| P698 | PubMed publication ID | 10448256 |
| P2093 | author name string | Greaves M | |
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| Concordance for Hodgkin's disease in identical twins suggesting genetic susceptibility to the young-adult form of the disease | Q46128221 | ||
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| A population-based study of multiple sclerosis in twins: update. | Q51053347 | ||
| In utero rearrangements in the trithorax-related oncogene in infant leukaemias. | Q52225004 | ||
| Chromosomal translocations in human cancer. | Q52512616 | ||
| A novel abl protein expressed in Philadelphia chromosome positive acute lymphoblastic leukaemia positive acute lymphoblastic leukaemia | Q59060532 | ||
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| Absence of p53 permits propagation of mutant cells following genotoxic damage | Q62127698 | ||
| Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening | Q69580527 | ||
| Identification of the constant chromosome regions involved in human hematologic malignant disease | Q70357868 | ||
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| p53 status and the efficacy of cancer therapy in vivo | Q72839445 | ||
| Age-specific incidence of acute lymphoblastic leukemia in U.S. children: in utero initiation model | Q73804658 | ||
| Loops, lineage, and leukemia | Q74800173 | ||
| PRENATAL ORIGIN OF CHILDHOOD LEUKEMIA. EVIDENCE FROM TWINS | Q76724439 | ||
| Oncogenesis in utero: fetal death due to acute myelogenous leukaemia with an MLL translocation | Q77597706 | ||
| Possible explanation of the high concoddance for acute leukaemia in monozygotic twins | Q93699150 | ||
| P433 | issue | 2 | |
| P921 | main subject | leukemia | Q29496 |
| P304 | page(s) | 173-185 | |
| P577 | publication date | 1999-02-01 | |
| P1433 | published in | European Journal of Cancer | Q332260 |
| P1476 | title | Molecular genetics, natural history and the demise of childhood leukaemia | |
| P478 | volume | 35 |
| Q73634028 | A fluorescence in situ hybridization study of TEL-AML1 fusion gene in B-cell acute lymphoblastic leukemia (1984-2001) |
| Q36672134 | A primitive cell origin for B-cell precursor ALL? |
| Q57985070 | ASSOCIATION BETWEENDEFB1GENE HAPLOTYPE AND HERPES VIRUSES SEROPREVALENCE IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA |
| Q58481810 | Acute Lymphoblastic Leukemia |
| Q92155277 | Are Leukaemic Stem Cells Restricted to a Single Cell Lineage? |
| Q36643873 | Association of early life factors and acute lymphoblastic leukaemia in childhood: historical cohort study |
| Q28210411 | B-cell development in the presence of the MLL/AF4 oncoprotein proceeds in the absence of HOX A7 and HOX A9 expression |
| Q40640707 | Birth order and risk of childhood cancer in the Danish birth cohort of 1973-2010. |
| Q34065462 | Bone marrow-derived mesenchymal stem cells undergo JCV T-antigen mediated transformation and generate tumors with neuroectodermal characteristics |
| Q33808971 | Childhood leukaemia |
| Q47296510 | Clonal variation of the immunogenotype in relapsed ETV6/RUNX1-positive acute lymphoblastic leukemia indicates subclone formation during early stages of leukemia development |
| Q35448434 | Contribution of polymorphisms in IKZF1 gene to childhood acute leukemia: a meta-analysis of 33 case-control studies |
| Q37792821 | Cytogenetic instability in childhood acute lymphoblastic leukemia survivors. |
| Q41854152 | Genetic Variations of Tumor Necrosis Factor -α-308 and Lymphtoxin-α+252 in Non-Hodgkin Lymphoma and Acute Lymphoblastic Leukemia Patients |
| Q33887427 | Genetic susceptibility to childhood leukaemia |
| Q36642349 | Haemophilus influenzae type B vaccination and risk of childhood leukaemia in a vaccine trial in Finland |
| Q35665931 | Hidden aberrations diagnosed by interphase fluorescence in situ hybridisation and spectral karyotyping in childhood acute lymphoblastic leukaemia |
| Q50767297 | High incidence and unique features of antigen receptor gene rearrangements in TEL-AML1-positive leukemias. |
| Q38448439 | Identification of preleukemic precursors of hyperdiploid acute lymphoblastic leukemia in cord blood |
| Q46902760 | Incidence of additional genetic changes in the TEL and AML1 genes in DCOG and COALL-treated t(12;21)-positive pediatric ALL, and their relation with drug sensitivity and clinical outcome |
| Q34386231 | Infection and childhood leukemia: review of evidence |
| Q36391849 | Infection, immune responses and the aetiology of childhood leukaemia |
| Q40580771 | Is the timing of exposure to infection a major determinant of acute lymphoblastic leukaemia in Hong Kong? |
| Q90663147 | Lineage Decision-Making within Normal Haematopoietic and Leukemic Stem Cells |
| Q45347188 | Maternal acute lymphoctic leukemia with rearrangement of the mixed lineage leukemia gene occurring during pregnancy |
| Q38744459 | Mechanism of ETV6-RUNX1 Leukemia |
| Q35050402 | Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia |
| Q74327628 | Microclustering of TEL-AML1 translocation breakpoints in childhood acute lymphoblastic leukemia |
| Q40878223 | Morphological and molecular evidence of differentiation during etoposide-induced apoptosis in human lymphoblastoid cells |
| Q40721250 | Non-DNA-binding Ikaros isoform gene expressed in adult B-precursor acute lymphoblastic leukemia |
| Q52947994 | Non-response bias as a likely cause of the association between young maternal age at the time of delivery and the risk of cancer in the offspring. |
| Q35210004 | Origins of chromosome translocations in childhood leukaemia |
| Q38448938 | Pre-natal, clonal origin of acute lymphoblastic leukaemia in triplets |
| Q74408878 | Precursor-B-ALL with D(H)-J(H) gene rearrangements have an immature immunogenotype with a high frequency of oligoclonality and hyperdiploidy of chromosome 14 |
| Q73156477 | Prenatal origin of acute lymphoblastic leukaemia in children |
| Q42606642 | Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins. |
| Q34998698 | Presence of clone-specific markers at birth in children with acute lymphoblastic leukaemia |
| Q34258082 | Prospect for immunotherapy of acute lymphoblastic leukemia |
| Q31049694 | Protracted postnatal natural histories in childhood leukemia |
| Q35779725 | Role of the TEL-AML1 fusion gene in the molecular pathogenesis of childhood acute lymphoblastic leukaemia |
| Q73583887 | Screening for herpesvirus genomes in common acute lymphoblastic leukemia |
| Q74310422 | Space-time clustering of childhood lymphatic leukaemias and non-Hodgkin's lymphomas in Sweden |
| Q34573970 | Survival of B lineage leukemic cells: signals from the bone marrow microenvironment |
| Q36184058 | The 5-minute Apgar score as a predictor of childhood cancer: a population-based cohort study in five million children |
| Q58481910 | The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation |
| Q59904413 | The United Kingdom Childhood Cancer Study: objectives, materials and methods. UK Childhood Cancer Study Investigators |
| Q34325014 | The association between acute lymphoblastic leukemia in children and Helicobacter pylori as the marker for sanitation |
| Q34242579 | The incidence of childhood leukaemia in West Berkshire |
| Q33826389 | The management of patients with leukaemia: the role of cytogenetics in this molecular era. |
| Q78427194 | The utility of spectral karyotyping in the cytogenetic analysis of newly diagnosed pediatric acute lymphoblastic leukemia |
| Q38059885 | The versatile landscape of haematopoiesis: are leukaemia stem cells as versatile? |
| Q37823589 | The versatility of haematopoietic stem cells: implications for leukaemia |
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