33 results on '"Morel, Frédéric"'
Search Results
2. NUDT6 and NUDT9, two mitochondrial members of the NUDIX family, have distinct hydrolysis activities
3. Breakpoint heterogeneity in (2;3)(p15–23;q26) translocations involving EVI1 in myeloid hemopathies
4. Genetic causes of macrozoospermia and proposal for an optimized genetic diagnosis strategy based on sperm parameters
5. MLL partner genes in secondary acute lymphoblastic leukemia: Report of a new partner PRRC1 and review of the literature
6. Translocation t(2;7)(p11;q21) associated with the CDK6/IGK rearrangement is a rare but recurrent abnormality in B-cell lymphoproliferative malignancies
7. ETV6 fusion genes in hematological malignancies: A review
8. Complex and cryptic chromosomal rearrangements involving the MLL gene in acute leukemia: A study of 7 patients and review of the literature
9. Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders
10. Cytogenetics in pre-B and B-cell acute lymphoblastic leukemia: a study of 208 patients diagnosed between 1981 and 2008
11. Differing mechanisms of meiotic segregation in spermatozoa from three carriers of a pericentric inversion of chromosome 8
12. 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
13. Deletion size characterization of der(9) deletions in Philadelphia-positive chronic myeloid leukemia
14. Screening by fluorescence in situ hybridization for MLL status at diagnosis in 239 unselected patients with acute myeloblastic leukemia
15. Jumping translocations in multiple myeloma
16. A fluorescence in situ hybridization study of TEL- AML1 fusion gene in B-cell acute lymphoblastic leukemia (1984–2001)
17. Characterization and meiotic segregation of a supernumerary marker chromosome in sperm of infertile males: Case report and literature review
18. Isolated 5p isochromosome in myelodysplastic syndrome: Report of the first case
19. 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
20. RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature
21. 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
22. Translocation (10;17)(p15;q21) is a recurrent anomaly in acute myeloblastic leukemia
23. Cryptic 5′ MLL gene insertion in an X-chromosome in acute myeloblastic leukemia
24. Rearrangement of the MLL gene in acute myeloblastic leukemia: report of two rare translocations
25. X chromosome insertion in the MLL gene in a case of childhood acute myeloblastic leukemia
26. Insertion of chromosome 11 in chromosome 4 resulting in a 5′MLL-3′AF4 fusion gene in a case of adult acute lymphoblastic leukemia
27. Translocation (12;21) followed by insertion of chromosome 3 material in the derivative chromosome 12 in a case of childhood acute lymphoblastic leukemia
28. t(4;11)(q21;p15), including one complex translocation t(1;4;11)(p32;q21;p15), in adult T-cell acute lymphoblastic leukemia
29. AML1 amplification in a case of childhood acute lymphoblastic leukemia
30. Molecular cytogenetic analysis by genomic hybridization to determine the cause of recurrent miscarriage
31. A second case of secondary acute myeloblastic leukemia associated with the MLL–KIAA0284 fusion gene
32. Rearrangement of the RHOH gene in a case of splenic lymphoma with villous lymphocytes
33. Identification of a complex (11;17;15) translocation in acute promyelocytic leukemia
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