CARDS IN CASE-REPORT (100)
A case of Acute Lymphoblastic Leukemia with rare t(11;22)(q23;q13)
A case of Chronic Lymphocytic Leukemia (CLL) with a rare chromosome abnormality: t(1;14;6)(q21;q32;p21), a variant of t(6;14)(p21;q32).
A case of Down syndrome with acute lymphoblastic leukemia and t(8;14)(q11;q32)
A Case of Myelodysplastic Syndrome with a Translocation t(1;12)(p36;p13)
A case of myeloproliferative disorder with t(5;10)(q33;q21.2)
A case of pre-B ALL with t(8;14)(q11;q32)
A case of sole i(4)(p10) in myelodysplastic syndrome
A case of trisomy 8 and loss of the Y-chromosome as secondary aberrations in a ten year old boy with de novo AML FAB M2 and t(16;21)(q24;q22)
A de novo AML with a t(1;21)(p36;q22) in an elderly patient
A first case of adult secondary acute myeloid leukemia with the recurrent KMT2A-GAS7 fusion
A new case of acute lymphoblastic leukemia with der(X)t(X;8)(q28;q11.2)
A new case of Acute Myeloid Leukemia with semi-cryptic t(7;21)(p22;q22)
A new case of adult Acute Myeloid Leukemia with isolated tetrasomy 4p
A new case of adult Acute Myeloid Leukemia with t(3;3)(p24;q26)
A new case of dic(1;15) in essential thrombocythaemia with JAK2 V617F mutation
A new case of t(16;21)(q24;q22) in a secondary AML-M2 following breast cancer therapy
A new case of t(1;11)(q21;q23) in a child with M1 ANLL
A new case of t(4;12)(q12;p13) in a secondary acute myeloid leukemia with review of literature
A new case of t(5;14)(q31;q32) in a pediatric acute lymphoblastic leukemia presenting with hypereosinophilia
A new case of t(8;14)(q11;q32) in an acute lymphoblastic leukemia
A new case of translocation t(14;14)(q11;q32) in B lineage ALL
A novel chromosomal translocation (6;14) (p22;q32) in a case of precursor B-cell Acute Lymphoblastic Leukemia
A pediatric case of acute lymphoblastic leukemia with t(2;9)(q12;q34) (RANBP2/ABL1 fusion)
A t(4;12)(q11;p13) in a patient with coincident CLL at the same time of AML diagnosis
Acute myeloid leukemia with t(12;13)(p13;q12) and ETV6 involvement; Case report and review of literature
AML with t(7;21)(p22;q22) and 5q abnormality, a case report
Amplification of MLL gene in a new case of acute myeloid leukemia
Amplification of the MET/7q31 gene in a patient with myelodysplastic syndrome
An adult case of biphenotypic acute leukemia with t(6;14)(q25;q32)
B-cell acute lymphoblastic leukemia with t(2;9)(p11;p13) involving the immunoglobulin kappa locus (IGK) and PAX-5
Chromosomal translocation t(X;11)(q22;q23) involving the MLL gene
Chronic lymphocytic leukaemia/Small lymphocytic lymphoma (CLL/SLL) associated with translocation t(1;6)(p35;p25) as part of complex karyotype
Clinical Relevance of Normal Diploid Workflow in Microarray Analysis of Massively Aneuploid Genomes: Lessons from a Case of B-Lymphoblastic Leukemia
Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia
der(1;18)(q10;q10) in a patient with AML following essential thrombocythemia
der(1;18)(q10;q10) in a pediatric patient with cytopenias
der(6)t(1;6)(q21;p21) in myelofibrosis following polycythemia vera
Dic(1;15)(p11;p11) as a non-random abnormality in atypical MPD
Dic(1;15)(p11;p11) as a non-random abnormality in essential thrombocytemia
Dic(1;15)(p11;p11) as a non-random abnormality in Myelodysplasic syndrome
Dic(1;15)(p11;p11) as a non-random abnormality in Polycytemia Vera
Dicentric dic(7;9)(p11;p11): a new case in childhood ALL
Homogeneously Staining Region (HSR) harboring CMYC amplification in a patient with primary plasma cell leukemia
Insertion as an alternative mechanism of CBFB-MYH11 gene fusion in a new case of acute myeloid leukemia with an abnormal chromosome 16
inv(8)(p11.2q13) found in a patient with chronic myelomonocytic leukemia that progressed to acute myeloid leukemia
Inversion(11)(p15q22) as a secondary anomaly in a case of relapsed MDS-RAEB after unrelated donor hematopoietic cell transplantation
Isolated 1q21 rearrangement der(20)t(1;20)(q21;p13) with telomere involvement of 20p in a case of longstanding myelodysplastic syndrome
Isolated trisomy 2 is non-random and may be found in myelodysplastic syndrome and in acute myeloblastic leukaemia. Case 1
Isolated trisomy 2 is non-random and may be found in myelodysplastic syndrome and in acute myeloblastic leukaemia. Case 2
JMML evolving to AML in a 14-year-old male acquiring an additional i(X)(q10)
KMT2A-CBL Fusion Gene Resulting from del(11)(q23.3q23.3) Identified by Chromosome Microarray Analysis - second report in AML
Patient with t(4;12)(q11;p13) with therapy-related MDS and known history of stage II metastatic colorectal cancer
Pentasomy 21 as a sole abnormality in an atypical CML patient in chronic phase
Reciprocal translocation t(2;12)(q31;p13) in a case of CMML
Ring Chromosome 8 as a sole abnormality: An adverse prognostic indicator in Acute Myeloid Leukemia?
Second case of t(2;21)(q11.2;q22.3) in a child with T-cell acute lymphoblastic leukemia
t(11;14;19)(q23;q32;p13.1) with simultaneous KMT2A and IGH rearrangements
t(11;17)(p15;q21) involving the NUP98 gene is a rare event in adult acute myeloid leukemia.
t(14;20)(q11.2;q13.3) involving the T-cell receptor α/δ gene in a pediatric acute lymphoblastic leukemia B-cell type
t(16;21)(q24;q22) in therapy-related acute myelogenous leukemia arising from myelodysplastic syndrome
t(17;21)(q11.2;q22) as a sole aberration in acute myelomonocytic leukemia
t(1;16)(q11-12;q11) presented as a der(16)t(1;16) in a patient with acute lymphoblastic leukemia.
t(1;21)(p32;q22) as a non-random abnormality in AML M4
t(2;11)(q31;p15) in therapy related myeloid neoplasm: case report and review of literature
t(3;4)(p21;q34) as a sole anomaly in acute myeloid leukemia patient
t(3;5)(q25;q35) as a sole anomaly in acute myeloid leukemia patient
t(3;7)(q26;q21) as a secondary abnormality in MDS RAEB-2
t(4;11)(q23;p15) in paediatric early T cell precursor acute lymphoblastic leukemia.
t(4;12)(q11;p13) in an acute myeloid leukemia without maturation with myelodysplasia
t(6;17)(p21;p13) and acquisition of the Philadelphia chromosome translocation with p190 BCR-ABL1 transcript during the course of myelodysplastic syndrome
t(6;17)(p21;p13) associated with t(3;3)(q21;q26.2) in AML
t(6;22)(p21;q11.2) arising at second relapse in a patient with t(8;21)-positive acute myeloid leukemia
t(6;8)(q27;p12) in a new case "8p11 myeloproliferative syndrome"
t(8;13)(p12;q12) in an atypical chronic myeloid leukaemia case
T-cell acute lymphoblastic leukemia with t(4;11)(q23;p15) and NUP98/RAP1GDS1 gene fusion: Case report and review of literature
T-cell acute lymphoblastic leukemia with t(7;14)(p15;q11.2)/HOXA-TCRA/D and biallelic deletion of CDKN2A. Case report and literature review
The rare t(4;12)(q11;p13) in an elderly patient with de novo AML with multilineage dysplasia co-expressing stem cell markers
The t(2;12)(p12;p13), leading to the juxtaposition of the cyclin D2 CCND2 gene with the immunoglobulin kappa locus (IGK), defines a small subset of mantle cell lymphomas lacking cyclin D1 expression.
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 1
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 2
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 3
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 4
Translocation t(11;14)(q25;q11) associated with T-cell receptor alpha/delta gene rearrangement and ATM gene deletion in a patient with B-cell chronic lymphocytic leukaemia.
Translocation t(11;15)(q23;q14) detected in AML at first relapse
Translocation t(11;20)(p15;q11) detected in AML M0: A case report
Translocation t(1;3)(p36;p21) and other aberrations in a case of AML secondary to MDS
Translocation t(1;6)(p35;p25) in B-cell lymphoproliferative disorder with evolution to Diffuse Large B-cell Lymphoma
Translocation t(2;19)(p11;p12-p13) in childhood with acute myeloid leukemia
Translocation t(5;17)(q13;q21) as the sole cytogenetic anomaly in acute myeloid leukemia after chemotherapy and allogeneic bone marrow transplantation for AML-M4: a case report
Translocation t(5;6)(q33-34;q23) in an acute myelomonocytic leukemia patient
Translocation t(7;9)(q34;q32) found in pediatric T-cell Acute Lymphoblastic Leukemia
Translocation t(8;12)(q13;p13) in a case with acute leukemia of ambiguous lineage
Translocation t(8;14)(q24;q32) as a clue for the diagnosis of B cell prolymphocytic leukemia
Translocation t(8;9)(p12;q33) detected in cALL: A case report
Translocation t(X;20)(q13;q13.3) as a secondary chromosome abnormality in a patient with 5q-: a case report
Trisomy 16 and 18 in acute lymphoblastic leukemia patient with ETV6-RUNX1 rearrangement
Unbalanced rearrangement der(9;18)(p10;q10) and JAK2 V617F mutation in a patient with AML following post-polycythemic myelofibrosis
Unbalanced rearrangement der(9;18)(p10;q10) in a patient with polycythemia vera
Unbalanced rearrangement, der(9;18)(p10;q10) in a patient with myelodysplastic syndrome. Case 0002M.
Unbalanced rearrangement, der(9;18)(p10;q10) in a patient with myeloproliferative neoplasm. Case 0001M.