Dual-color interphase fluorescence in situ hybridization (FISH) with ETV6 and AML1 probes was used for the first time on a series of 159 adult patients with acute lymphoblastic leukemia (ALL), for detection of the t(12;21)(p13;q22) translocation. Seven patients (4.4%) were found, with 50-100% of positive cells, of whom one of two tested, proved negative for the fusion product by RT-PCR. Two of them, aged 43 and 50 years, are the oldest patients so far confirmed to have the translocation. Three who relapsed at 10, 11 and 24 months, suggest that adults may not enjoy the good short-term prognosis reported for t(12;21)-positive children. Thirty-one-negative cases had signal numbers differing from the two expected for each gene. In 15 cases thes...
Fluorescence in situ hybridization (FISH) and/or RNA-based polymerase chain reaction (RT-PCR) were u...
Reciprocal translocations involving the MLL gene on chromosome band 11q23 have been observed in both...
Rearrangements involving the MLL gene at 11q23 occur in a clinically relevant subgroup of patients w...
In a paper published in Leukemia in 2002, Jabbar Al-Obaidi and colleagues on behalf of the MRC Adult...
Translocation t(12;21)(p13;q22) is the most frequent cytogenetic abnormality in childhood acute lymp...
Translocation t(12;21)(p13;q22) is the most frequent cytogenetic abnormality in childhood acute lymp...
The translocation (8;21) is a chromosome abnormality associated with acute myeloid leukemia (AML). A...
While the MLL “recombinome” is relatively well characterized in B-cell precursor acute lymphoblastic...
To validate a 2-step FISH assay for the identification of the t(9;11)(p22;q23), 96 acute myeloid leu...
To validate a 2-step FISH assay for the identification of the t(9;11)(p22;q23), 96 acute myeloid leu...
The t(7;12)(q36;p13) translocation is a recurrent chromosome abnormality that involves the ETV6 gene...
In the last decade molecular cytogenetics, or fluorescence in situ hybridization (FISH), has become ...
The value of dual-color fluorescence in situ hybridization (FISH) for the detection of inv(16), usin...
Rearrangements involving the MLL gene at 11q23 occur in a clinically relevant subgroup of patients w...
This study describes the cytogenetics of 33 children with ETV6-RUNX1 positive acute lymphoblastic le...
Fluorescence in situ hybridization (FISH) and/or RNA-based polymerase chain reaction (RT-PCR) were u...
Reciprocal translocations involving the MLL gene on chromosome band 11q23 have been observed in both...
Rearrangements involving the MLL gene at 11q23 occur in a clinically relevant subgroup of patients w...
In a paper published in Leukemia in 2002, Jabbar Al-Obaidi and colleagues on behalf of the MRC Adult...
Translocation t(12;21)(p13;q22) is the most frequent cytogenetic abnormality in childhood acute lymp...
Translocation t(12;21)(p13;q22) is the most frequent cytogenetic abnormality in childhood acute lymp...
The translocation (8;21) is a chromosome abnormality associated with acute myeloid leukemia (AML). A...
While the MLL “recombinome” is relatively well characterized in B-cell precursor acute lymphoblastic...
To validate a 2-step FISH assay for the identification of the t(9;11)(p22;q23), 96 acute myeloid leu...
To validate a 2-step FISH assay for the identification of the t(9;11)(p22;q23), 96 acute myeloid leu...
The t(7;12)(q36;p13) translocation is a recurrent chromosome abnormality that involves the ETV6 gene...
In the last decade molecular cytogenetics, or fluorescence in situ hybridization (FISH), has become ...
The value of dual-color fluorescence in situ hybridization (FISH) for the detection of inv(16), usin...
Rearrangements involving the MLL gene at 11q23 occur in a clinically relevant subgroup of patients w...
This study describes the cytogenetics of 33 children with ETV6-RUNX1 positive acute lymphoblastic le...
Fluorescence in situ hybridization (FISH) and/or RNA-based polymerase chain reaction (RT-PCR) were u...
Reciprocal translocations involving the MLL gene on chromosome band 11q23 have been observed in both...
Rearrangements involving the MLL gene at 11q23 occur in a clinically relevant subgroup of patients w...