Publication date
January 2019
DOI Publisher
INIST-CNRS Journal
Atlas of Genetics and Cytogenetics in Oncology and HaematologyAbstract
A novel TBL1XR1/MECOM fusion was identified in a patient with acute undifferentiated leukemia
A novel TBL1XR1/MECOM fusion was identified in a patient with acute undifferentiated leukemia
8p11 myeloproliferative syndrome is a rare hematological malignancy with aggressive course caused by...
SummaryTo identify oncogenic pathways in T cell acute lymphoblastic leukemia (T-ALL), we combined ex...
AbstractMLL gene aberrations are frequently diagnosed in infant acute myeloid leukemia (AML). We pre...
A novel CUX1-NUTM1 fusion identified in B-cell precursor acute lymphoblastic leukemia
De Braekeleer et al.1 published the first case of acute lymphoblastic leukemia (ALL) associated with...
Review on t(3;5)(q26;q31) H2AFY/MECOM, with data on clinics, and the genes involved
International audienceBackground: A large number of chromosomal translocations of the human KMT2A ge...
Review on del(11)(q23q23) MLL/CBL - t(11;11)(q23;q23) MLL/CBL, with data on clinics, and the genes i...
Background: Abnormalities of 11q23 involving the MLL gene are found in approximately 10% of human le...
A novel NUMA1/PDGFRB fusion identified in B-cell precursor acute lymphoblastic leukemia is described
© 2001 Hussey et al; licensee BioMed Central Ltd. Verbatim copying and redistribution of this articl...
Chromosomal rearrangements of the human MLL/KMT2A gene are associated with infant, pediatric, adult ...
In the last years, collaborative studies have joined to link the degree of genetic heterogeneity of ...
In a case of acute myeloid leukemia we report molecular cytogenetic findings of a t(3;11)(q12;p15), ...
We present a novel, rare but recurrent variant three way translocation of t(8;21), t(8;16;21)(q22;q2...
8p11 myeloproliferative syndrome is a rare hematological malignancy with aggressive course caused by...
SummaryTo identify oncogenic pathways in T cell acute lymphoblastic leukemia (T-ALL), we combined ex...
AbstractMLL gene aberrations are frequently diagnosed in infant acute myeloid leukemia (AML). We pre...
A novel CUX1-NUTM1 fusion identified in B-cell precursor acute lymphoblastic leukemia
De Braekeleer et al.1 published the first case of acute lymphoblastic leukemia (ALL) associated with...
Review on t(3;5)(q26;q31) H2AFY/MECOM, with data on clinics, and the genes involved
International audienceBackground: A large number of chromosomal translocations of the human KMT2A ge...
Review on del(11)(q23q23) MLL/CBL - t(11;11)(q23;q23) MLL/CBL, with data on clinics, and the genes i...
Background: Abnormalities of 11q23 involving the MLL gene are found in approximately 10% of human le...
A novel NUMA1/PDGFRB fusion identified in B-cell precursor acute lymphoblastic leukemia is described
© 2001 Hussey et al; licensee BioMed Central Ltd. Verbatim copying and redistribution of this articl...
Chromosomal rearrangements of the human MLL/KMT2A gene are associated with infant, pediatric, adult ...
In the last years, collaborative studies have joined to link the degree of genetic heterogeneity of ...
In a case of acute myeloid leukemia we report molecular cytogenetic findings of a t(3;11)(q12;p15), ...
We present a novel, rare but recurrent variant three way translocation of t(8;21), t(8;16;21)(q22;q2...
8p11 myeloproliferative syndrome is a rare hematological malignancy with aggressive course caused by...
SummaryTo identify oncogenic pathways in T cell acute lymphoblastic leukemia (T-ALL), we combined ex...
AbstractMLL gene aberrations are frequently diagnosed in infant acute myeloid leukemia (AML). We pre...
Add to ORKG