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Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia

Blood cells, molecules, & diseases, 2008-05, Vol.40 (3), p.452-455

2008

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Broad molecular screening of an unclassifiable myeloproliferative disorder reveals an unexpected ETV6 ABL1 fusion transcript

Leukemia, 2005-06, Vol.19 (6), p.1096-1099

2005

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Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia

Leukemia, 2006-02, Vol.20 (2), p.247-253

2006

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Systemic mastocytosis with associated myeloproliferative disease and precursor B lymphoblastic leukaemia with t(13;13)(q12;q22) involving FLT3

Journal of clinical pathology, 2008-08, Vol.61 (8), p.958-961

2008

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Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

Oncogene, 1999-01, Vol.18 (2), p.543-550

1999

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A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia : dic(9;20)(p1?3;q11)

Leukemia, 1995-10, Vol.9 (10), p.1613-1619

1995

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Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia

Leukemia, 1996-09, Vol.10 (9), p.1459-1462

1996

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Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML)

Leukemia, 1997-07, Vol.11 (7), p.964-970

1997

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Fluorescent in situ hybridization (FISH), cytogenetic analytical complement for the diagnosis of malignant blood diseases

Revue medicale de la Suisse romande, 2000-05, Vol.120 (5), p.393

2000

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A novel BCR‐ABL transcript e2a2 in a chronic myelogenous leukaemia patient with a duplicated Ph‐chromosome and monosomy 7

British journal of haematology, 1999-09, Vol.106 (4), p.1041-1044

1999

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Cytogenetics of malignant hemopathies

Revue medicale de la Suisse romande, 1993-04, Vol.113 (4), p.291

1993

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RT-PCR Diagnosis of Patients With Acute Nonlymphocytic Leukemia and inv(16)(pl3q22) and Identification of New Alternative Splicing in CBFB-MYH11 Transcripts

Blood, 1995-07, Vol.86 (1), p.277-282

1995

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Effect of Conditioned Medium, Nutritive Elements and Mitotic Synchronization on the Accuracy of the Cytogenetic Analysis in Patients with Chronic Myeloid Leukemia at Diagnosis and During α-Interferon Therapy

Cancer genetics and cytogenetics, 1999-03, Vol.109 (2), p.166-171

1999

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A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL)

Blood, 2002-09, Vol.100 (5), p.1787-1794

2002

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Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome

Cancer genetics and cytogenetics, 1992-04, Vol.59 (2), p.138-160

1992

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t(8;9)(p11;q32) IN ATYPICAL CHRONIC MYELOID LEUKAEMIA: A NEW CYTOGENETTC‐CLINICOPATHOLOGIC ASSOCIATION?

British journal of haematology, 1992-06, Vol.81 (2), p.307-308

1992

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Frequent clonal loss of heterozygosity but scarcity of microsatellite instability at chromosomal breakpoint cluster regions in adult leukemias

Blood, 1996-08, Vol.88 (3), p.1026-1034

1996

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Frequent Clonal Loss of Heterozygosity but Scarcity of Microsatellite Instability at Chromosomal Breakpoint Cluster Regions in Adult Leukemias

Blood, 1996-08, Vol.88 (3), p.1026-1034

1996

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Two clonal occurrences of tetrasomy 21 in an atypical chronic myeloid leukemia with wild-type RUNX1 alleles. Additional support for a gene dosage effect of chromosome 21 or RUNX1 in leukemia

Haematologica (Roma), 2004-08, Vol.89 (8), p.ECR26

2004

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Short-term culture of spleen lymphocytes for chromosome analysis of small rodents

Genetica, 1990-12, Vol.83 (1), p.51-60

1990

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t(8;9) IN CHRONIC MYELOID LEUKAEMIA

British journal of haematology, 1993-01, Vol.83 (1), p.176-177

1993

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t(8;9)(p11;q32) in atypical chronic myeloid leukaemia : a new cytogenetic-clinicopathologic association ?

British journal of haematology, 1992-06, Vol.81 (2), p.307-308

1992

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Tetrasomy 8 in a patient with acute nonlymphocytic leukemia: A metaphase and interphase study with fluorescence in situ hybridization

Cancer genetics and cytogenetics, 1996-07, Vol.89 (1), p.44-48

1996

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Effect of conditioned media, nutritive elements, and mitotic synchronization on the accuracy of the cytogenetic analysis in acute nonlymphocytic leukemia patients presenting with inv(16)/t(16;16) or t(15;17)

Cancer genetics and cytogenetics, 1997-04, Vol.94 (2), p.106-112

1997

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Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia

Broad molecular screening of an unclassifiable myeloproliferative disorder reveals an unexpected ETV6 ABL1 fusion transcript

Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia

Systemic mastocytosis with associated myeloproliferative disease and precursor B lymphoblastic leukaemia with t(13;13)(q12;q22) involving FLT3

Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia : dic(9;20)(p1?3;q11)

Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia

Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML)

Fluorescent in situ hybridization (FISH), cytogenetic analytical complement for the diagnosis of malignant blood diseases

A novel BCR‐ABL transcript e2a2 in a chronic myelogenous leukaemia patient with a duplicated Ph‐chromosome and monosomy 7

Cytogenetics of malignant hemopathies

RT-PCR Diagnosis of Patients With Acute Nonlymphocytic Leukemia and inv(16)(pl3q22) and Identification of New Alternative Splicing in CBFB-MYH11 Transcripts

Effect of Conditioned Medium, Nutritive Elements and Mitotic Synchronization on the Accuracy of the Cytogenetic Analysis in Patients with Chronic Myeloid Leukemia at Diagnosis and During α-Interferon Therapy

A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL)

Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome

t(8;9)(p11;q32) IN ATYPICAL CHRONIC MYELOID LEUKAEMIA: A NEW CYTOGENETTC‐CLINICOPATHOLOGIC ASSOCIATION?

Frequent clonal loss of heterozygosity but scarcity of microsatellite instability at chromosomal breakpoint cluster regions in adult leukemias

Frequent Clonal Loss of Heterozygosity but Scarcity of Microsatellite Instability at Chromosomal Breakpoint Cluster Regions in Adult Leukemias

Two clonal occurrences of tetrasomy 21 in an atypical chronic myeloid leukemia with wild-type RUNX1 alleles. Additional support for a gene dosage effect of chromosome 21 or RUNX1 in leukemia

Short-term culture of spleen lymphocytes for chromosome analysis of small rodents

t(8;9) IN CHRONIC MYELOID LEUKAEMIA

t(8;9)(p11;q32) in atypical chronic myeloid leukaemia : a new cytogenetic-clinicopathologic association ?

Tetrasomy 8 in a patient with acute nonlymphocytic leukemia: A metaphase and interphase study with fluorescence in situ hybridization

Effect of conditioned media, nutritive elements, and mitotic synchronization on the accuracy of the cytogenetic analysis in acute nonlymphocytic leukemia patients presenting with inv(16)/t(16;16) or t(15;17)

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