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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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Dicentric Translocation (9;12) Presenting as Refractory Philadelphia Chromosome-Positive Acute B-Cell Lymphoblastic Leukemia

Cancer genetics and cytogenetics, 1999-08, Vol.113 (1), p.90-92

1999

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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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Cytogenetics of malignant hemopathies

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

1993

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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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Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases

Cancer genetics and cytogenetics, 2005-07, Vol.160 (2), p.97-119

2005

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Systematic screening at diagnosis of −5/del(5)(q31), −7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics

Cancer genetics and cytogenetics, 2004-07, Vol.152 (1), p.29-41

2004

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Determination of cutoff values to detect small aneuploid clones by interphase fluorescence in situ hybridization: the Poisson model is a more appropriate approach. Should single-cell trisomy 8 be considered a clonal defect?

Cancer genetics and cytogenetics, 2003-12, Vol.147 (2), p.99-109

2003

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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)

Dicentric Translocation (9;12) Presenting as Refractory Philadelphia Chromosome-Positive Acute B-Cell Lymphoblastic Leukemia

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

Cytogenetics of malignant hemopathies

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

Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases

Systematic screening at diagnosis of −5/del(5)(q31), −7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics

Determination of cutoff values to detect small aneuploid clones by interphase fluorescence in situ hybridization: the Poisson model is a more appropriate approach. Should single-cell trisomy 8 be considered a clonal defect?

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