265 results on '"Le Bris, Marie-Josée"'
Search Results
2. MLL partner genes in secondary acute lymphoblastic leukemia: Report of a new partner PRRC1 and review of the literature
3. Translocation t(2;7)(p11;q21) associated with the CDK6/IGK rearrangement is a rare but recurrent abnormality in B-cell lymphoproliferative malignancies
4. ETV6 fusion genes in hematological malignancies: A review
5. Identification of MLL partner genes in 27 patients with acute leukemia from a single cytogenetic laboratory
6. Complex and cryptic chromosomal rearrangements involving the MLL gene in acute leukemia: A study of 7 patients and review of the literature
7. Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders
8. Cytogenetics in pre-B and B-cell acute lymphoblastic leukemia: a study of 208 patients diagnosed between 1981 and 2008
9. Translocations involving 13q14 without associated deletion in chronic lymphoid leukaemia target DLEU2
10. Distinct clonal anomalies involving RUNX1 in acute myeloid leukemia at diagnosis and after bone marrow transplantation
11. A combination therapy with fludarabine, mitoxantrone and rituximab induces complete immunophenotypical remission in B-cell prolymphocytic leukaemia
12. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions
13. Del(5q) and MLL amplification in homogeneously staining region in acute myeloblastic leukemia: a recurrent cytogenetic association
14. Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions
15. Deletion size characterization of der(9) deletions in Philadelphia-positive chronic myeloid leukemia
16. Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: Molecular characterization of two der(11)t(11;16)
17. A complex 1;19;11 translocation involving the MLL gene in a patient with congenital acute monoblastic leukemia identified by molecular and cytogenetic techniques
18. Balanced transmission of a paternal complex chromosomal rearrangement involving chromosomes 2, 3, and 18
19. FLNA, a new partner gene fused to MLL in a patient with acute myelomonoblastic leukaemia
20. Diagnosis and outcome of complete hydatidiform mole coexisting with a live twin fetus
21. Screening by fluorescence in situ hybridization for MLL status at diagnosis in 239 unselected patients with acute myeloblastic leukemia
22. Jumping translocations in multiple myeloma
23. Molecular cytogenetic characterization of an 8p22–8p23.2 duplication derived from a maternal intrachromosomal insertion in a child with congenital heart malformation, delayed puberty, and learning disabilities
24. Familial interstitial deletion of the short arm of chromosome 4 (p15.33–p16.3) characterized by molecular cytogenetic analysis
25. Second-trimester prenatal screening for trisomy 21 using biochemical markers: a 7-year experience in one cytogenetic laboratory
26. Meiotic segregation of translocations during male gametogenesis
27. Double minutes containing amplified bcr-abl fusion gene in a case of chronic myeloid leukemia treated by imatinib
28. A fluorescence in situ hybridization study of TEL- AML1 fusion gene in B-cell acute lymphoblastic leukemia (1984–2001)
29. An increased incidence of autosomal aneuploidies in spermatozoa from a patient with Klinefelter’s syndrome
30. Characterization and meiotic segregation of a supernumerary marker chromosome in sperm of infertile males: Case report and literature review
31. Using Bacterial Artificial Chromosomes in Leukemia Research: The Experience at the University Cytogenetics Laboratory in Brest, France
32. Immunoglobulin gene translocations in chronic lymphocytic leukemia: A report of 35 patients and review of the literature
33. Jumping translocation involving 13q34 in chronic lymphocytic leukemia: report of the first case studied by fluorescentin situhybridization
34. Incidence of Chromosomal Anomalies Detected by Interphase Fish in Chronic Lymphoid Leukemia
35. 3q26/EVI1 rearrangements in myeloid hemopathies: a cytogenetic review
36. Translocations involving 13q14 without associated deletion in chronic lymphoid leukaemia targetDLEU2
37. Isolated 5p isochromosome in myelodysplastic syndrome: Report of the first case
38. Three rearrangements of chromosome 5 in a patient with myelodysplastic syndrome: an atypical deletion 5q, a complex intrachromosomal rearrangement of chromosome 5, and a paracentric inversion of chromosome 5
39. A novel translocation (6;20)(q13;q12) in acute myeloid leukemia likely results inLMBRD1–CHD6fusion
40. Recurrent translocation (10;17)(p15;q21) in acute poorly differentiated myeloid leukemia likely results inZMYND11–MBTD1fusion
41. RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature
42. Distinct clonal deletions of the long arm of chromosome 5 in a patient with myelodysplastic syndrome
43. Identification ofMLLpartner genes in 27 patients with acute leukemia from a single cytogenetic laboratory
44. RUNX1 translocations and fusion genes in malignant hemopathies
45. DIFFICULT DIAGNOSIS AND MANAGEMENT OF AN HETEROKARYOTYPIC MONOCHORIONIC TWIN PREGNANCY WITH DISCORDANT FETAL SEX AND 45,X/47,XYY KAROTYPES
46. Identification of aMLL–MLLT4fusion gene resulting from a t(6;11)(q27;q23) presenting as a del(11q) in a child with T-cell acute lymphoblastic leukemia
47. RUNX1amplification in B-cell acute lymphoblastic leukemia
48. FLNA, a new partner gene fused toMLLin a patient with acute myelomonoblastic leukaemia
49. A second case of secondary acute myeloblastic leukemia associated with the MLL–KIAA0284 fusion gene
50. Translocation 3;21, trisomy 8, and duplication of the Philadelphia chromosome: a rare but recurrent cytogenetic pathway in the blastic phase of chronic myeloid leukemia
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