Complex translocation (6;21;8), a variant of t(8;21), with trisomy 4 in a patient with acute myelogenous leukemia (M2).

[1]  E. Soeda,et al.  Alternative splicing and genomic structure of the AML1 gene involved in acute myeloid leukemia. , 1995, Nucleic acids research.

[2]  N. Kamada,et al.  Junctions of the AML1/MTG8(ETO) fusion are constant in t(8;21) acute myeloid leukemia detected by reverse transcription polymerase chain reaction. , 1993, Blood.

[3]  M. Ohki,et al.  The 8;21 chromosome translocation in acute myeloid leukemia is always detectable by molecular analysis using AML1 , 1993 .

[4]  J. Rowley,et al.  Detection of DNA rearrangements in the AML1 and ETO loci and of an AML1/ETO fusion mRNA in patients with t(8;21) acute myeloid leukemia. , 1993, Blood.

[5]  F. Calabi,et al.  Translocation breakpoints are clustered on both chromosome 8 and chromosome 21 in the t(8;21) of acute myeloid leukemia. , 1993, Blood.

[6]  H. Drabkin,et al.  Identification of breakpoints in t(8;21) acute myelogenous leukemia and isolation of a fusion transcript, AML1/ETO, with similarity to Drosophila segmentation gene, runt. , 1992, Blood.

[7]  M. Ohki,et al.  t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[8]  J. Rowley,et al.  Recurring chromosome abnormalities in leukemia and lymphoma. , 1990, Seminars in hematology.

[9]  O. Haas,et al.  Trisomy 4: a specific karyotype anomaly in primary and secondary acute myeloid leukemia. , 1990, Leukemia.

[10]  Groupe Français de Cytogénétique Hématologique Acute myelogenous leukemia with an 8;21 translocation. A report on 148 cases from the Groupe Français de Cytogénétique Hématologique. , 1990, Cancer genetics and cytogenetics.

[11]  R. Beuscart,et al.  Cytogenetics and their prognostic value in de novo acute myeloid leukaemia: a report on 283 cases , 1989, British journal of haematology.

[12]  M. Minamihisamatsu,et al.  Translocation (8;21) and its variants in acute nonlymphocytic leukemia. The relative importance of chromosomes 8 and 21 to the genesis of the disease. , 1988, Cancer genetics and cytogenetics.

[13]  F. Sigaux,et al.  Prognostic significance of chromosomal abnormalities in acute nonlymphocytic leukemia: a study of 343 patients. , 1987, Cancer genetics and cytogenetics.

[14]  F. Hecht,et al.  Trisomy 4 in hematologic disorders. , 1987, Cancer Genetics and Cytogenetics.

[15]  H. Taguchi,et al.  New variant translocation (1;8;21) in a case of acute myeloblastic leukemia (M2). , 1986, Cancer genetics and cytogenetics.

[16]  G. Tricot,et al.  Trisomy-4 Identifies a Subset of Acute Nonlymphocytic Leukemias , 1986 .

[17]  G Flandrin,et al.  Proposed revised criteria for the classification of acute myeloid leukemia. A report of the French-American-British Cooperative Group. , 1985, Annals of internal medicine.

[18]  S. Raynaud,et al.  Variant translocation t(8;21;15) in an acute myeloblastic leukemia with phenotypic differential evolution. , 1985, Cancer genetics and cytogenetics.

[19]  O. Garson,et al.  Translocation (8;21)(q22;q22) in Acute Nonlymphocytic Leukemia , 1984 .

[20]  J. Testa,et al.  A variant 8;21 translocation in acute myeloblastic leukemia , 1983, American journal of hematology.