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ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7

Haematologica (Roma), 2012-12, Vol.97 (12), p.1933-1936

2012

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Detection of chromosome abnormalities using cytoplasmic immunoglobulin staining and FISH in myeloma

Methods in molecular biology (Clifton, N.J.), 2011, Vol.730, p.159

2011

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Appearance of del(11q) in two patients with acute promyelocytic leukaemia treated with all‐trans retinoic acid and combination chemotherapy

British journal of haematology, 2002-07, Vol.118 (1), p.243-245

2002

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Gene amplification in myeloid leukemias elucidated by fluorescence in situ hybridization

Cancer genetics and cytogenetics, 2009-08, Vol.193 (1), p.44-53

2009

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BCR/ABL amplification in chronic myelocytic leukemia blast crisis following imatinib mesylate administration

Cancer genetics and cytogenetics, 2002-11, Vol.139 (1), p.30-33

2002

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Frequent loss of heterozygosity in early non‐small cell lung cancers at chromosome 9p21 proximal to the CDKN2a gene

International journal of cancer, 1997-04, Vol.71 (2), p.213-217

1997

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546 A potential second tumour suppressor gene locus located at chromosome 9p21 in non-small cell lung cancer

Lung cancer (Amsterdam, Netherlands), 1997-08, Vol.18, p.140-140

1997

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MYC Amplification in Two Further Cases of Acute Myeloid Leukemia with Trisomy 4 and Double Minute Chromosomes

Cancer genetics and cytogenetics, 1999-03, Vol.109 (2), p.123-125

1999

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Physical Mapping of a Tandem Duplication on the Long Arm of Chromosome 7 Associated with a Multidrug Resistant Phenotype

Cancer genetics and cytogenetics, 1999-04, Vol.110 (1), p.28-33

1999

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ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7

Dynamic molecular monitoring reveals that SWI-SNF mutations mediate resistance to ibrutinib plus venetoclax in mantle cell lymphoma

Detection of chromosome abnormalities using cytoplasmic immunoglobulin staining and FISH in myeloma

Appearance of del(11q) in two patients with acute promyelocytic leukaemia treated with all‐trans retinoic acid and combination chemotherapy

Gene amplification in myeloid leukemias elucidated by fluorescence in situ hybridization

BCR/ABL amplification in chronic myelocytic leukemia blast crisis following imatinib mesylate administration

Frequent loss of heterozygosity in early non‐small cell lung cancers at chromosome 9p21 proximal to the CDKN2a gene

546 A potential second tumour suppressor gene locus located at chromosome 9p21 in non-small cell lung cancer

MYC Amplification in Two Further Cases of Acute Myeloid Leukemia with Trisomy 4 and Double Minute Chromosomes

Physical Mapping of a Tandem Duplication on the Long Arm of Chromosome 7 Associated with a Multidrug Resistant Phenotype

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