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Journal Articles

Clinical and Cytogenomic Features of Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 (iAMP21) in the Context of Constitutional Ring Chromosome 21

Tatiana Tvrdik, PhD MSc, Kristian T. Schafernak, MD MPH, Jeffrey R Jacobsen, MD, Reha Toydemir, MD PhD, Alexandra M Walsh, MD, Bo Hong, MD

Blood (2019) 134 (Supplement_1): 5208.

https://doi.org/10.1182/blood-2019-123766

Published: 2019

Journal Articles

Constitutional Ring Chromosome 21 Predisposes to Acute Lymphoblastic Leukaemia (ALL) with iAMP21

Claire Schwab, Eigil Kjeldsen, MD DMSc, Nyla A. Heerema, PhD, Andrew Carroll, PhD, Matthew Bashton, PhD, Sarra Ryan, PhD, Anthony V. Moorman, PhD, Stephen P. Hunger, MD, Mignon L. Loh, MD, Henrik Hasle, MD PhD, Christine J Harrison, PhD FRCPath

Blood (2017) 130 (Supplement 1): 3978.

https://doi.org/10.1182/blood.V130.Suppl_1.3978.3978

Published: 2017

Journal Articles

Patient Characteristics and Early Death Predictors in Acute Promyelocytic Leukaemia Patients; Experience from United Arab Emirates (UAE)

Mariam Rashed Alzaabi, MBBS, Inaam bashir Hassan, MBBS, PhD, Martin S Tallman, MD, Arif Alam, MBBS, Khalid Al qawasmeh, Jorgen Kristensen, MD PhD

Blood (2015) 126 (23): 4963.

https://doi.org/10.1182/blood.V126.23.4963.4963

Published: 2015

Journal Articles

Prognostic Impact Of a Newly Defined Structurally Complex Karyotype In Patients With AML and MDS After Allogeneic Stem Cell Transplantation

Christiane E Dobbelstein, MD, Elke Dammann, Eva M Weissinger, MD, Michael Stadler, MD, Matthias Eder, MD, Brigitte Schlegelberger, MD, PhD, Arnold Ganser, MD, Gudrun Gohring, MD

Blood (2013) 122 (21): 3362.

https://doi.org/10.1182/blood.V122.21.3362.3362

Published: 2013

Journal Articles

Gene Amplifications In 84 Patients With Acute Myeloid Leukemia and 31 Patients With Myelodysplastic Syndrome Investigated By Array CGH

Andreas Roller, PhD, Simone Weber, Alexander Kohlmann, PhD, Melanie Zenger, Marita Staller, Wolfgang Kern, MD, Susanne Schnittger, PhD, Torsten Haferlach, MD, Claudia Haferlach, MD

Blood (2013) 122 (21): 3724.

https://doi.org/10.1182/blood.V122.21.3724.3724

Published: 2013

Journal Articles

Monosomal Karyotype Is Associated With Worse Survival Independent Of Complex Karyotype In Patients With Myelodysplastic Syndrome

Zoe K McQuilten, MBBS, Vijaya Sundararajan, MD, Erica M Wood, MBBS, David J. Curtis, M.D., Ph.D., Mark N Polizzotto, MBBS, BMedSc, Lynda J Campbell, MBBS, Meaghan Wall, MBBS (Hons), FRACP, FRCPA, PhD

Blood (2013) 122 (21): 1523.

https://doi.org/10.1182/blood.V122.21.1523.1523

Published: 2013

Journal Articles

RUNX1 Deletions Are a Novel Mechanism of Loss of Function in AML and Are Associated with Adverse Cytogenetics.

Claudia Haferlach, MD, Vera Grossmann, MSc, Melanie Zenger, Wolfgang Kern, MD, Torsten Haferlach, MD, Alexander Kohlmann, PhD, Susanne Schnittger, PhD

Blood (2012) 120 (21): 2517.

https://doi.org/10.1182/blood.V120.21.2517.2517

Published: 2012

Journal Articles

Intrachromosomal Amplification of Chromosome 21(iAMP21): Cytogenetic Characterisation and Outcome in Childhood B-Cell Precursor Acute Lymphoblastic Leukaemia (BCP-ALL). A Study On Behalf of the Ponte Di Legno International Childhood ALL Workshop

Christine J Harrison, PhD, FRCPath, Anthony V. Moorman, PhD, Claire Schwab, BSc, Nyla A. Heerema, PhD, Andrew J. Carroll, PhD, Oskar A. Haas, MD

Blood (2012) 120 (21): 293.

https://doi.org/10.1182/blood.V120.21.293.293

Published: 2012

Journal Articles

Thrombocytopenia and Platelet Ultra-Structural Abnormalities Associated with RUNX1 Haploinsufficiency in Monosomy 21 Mosaicism.

Riten Kumar, MD, MSc, Fred Pluthero, PhD, Hilary Christensen, Walter H. Kahr, MD, PhD

Blood (2012) 120 (21): 2190.

https://doi.org/10.1182/blood.V120.21.2190.2190

Published: 2012

Journal Articles

SNP-A Karyotyping Provides Clinically Relevant Results In Myeloid Hematologic Disorders with Unsuccessful Routine Cytogenetic Testing.

Kathryn M Guinta, Hideki Makishima, MD, PhD, Christine L. O'Keefe, PhD, Simon Dujardin, Ramon V. Tiu, MD, Mikkael A. Sekeres, MD, MS, Jaroslaw P Maciejewski, MD, PhD, FACP

Blood (2010) 116 (21): 3374.

https://doi.org/10.1182/blood.V116.21.3374.3374

Published: 2010

Journal Articles

Atypical Cytogenetic Findings Detected by Whole Genomic Microarray Analysis In Pediatric Acute Lymphoblastic Leukemia Cases

Feng Li, MD, PhD, Xu Li, MD, PhD, Lauren Jenkins, PhD, Vincent A. Kiley, MD

Blood (2010) 116 (21): 4862.

https://doi.org/10.1182/blood.V116.21.4862.4862

Published: 2010

Journal Articles

Acute Lymphoblastic Leukemia in a Case of Ring Chromosome

Seval Türkmen, Sebastian Muller, Stefan Mundlos, Günter Henze, Holger Lode

Blood (2008) 112 (11): 4151.

https://doi.org/10.1182/blood.V112.11.4151.4151

Published: 2008

Journal Articles

Genome Complexity in Patients with Acute Lymphoblastic Leukaemia Revealed by Array-Based Comparative Genomic Hybridization.

Jon C. Strefford, PhD, Helen Worley, B.Sc., Kerry Barber, B.Sc., Anthony V. Moorman, Ph.D., Christine J. Harrison, Ph.D.

Blood (2006) 108 (11): 2061.

https://doi.org/10.1182/blood.V108.11.2061.2061

Published: 2006

Journal Articles

Cytogenetic Classification of T Lineage Acute Lymphoblastic Leukaemia: Multiple Partners of BCL11B and Other Novel Rearrangements.

Christine J. Harrison, PhD, Kerry Barber, Zoë Broadfield, Adam Stewart, Sarah Wright, Mary Martineau, PhD, Jon C. Strefford, PhD, Anthony V. Moorman, PhD

Blood (2006) 108 (11): 2062.

https://doi.org/10.1182/blood.V108.11.2062.2062

Published: 2006

Journal Articles

Translocation t(Y;14)(q12;q11): A New Abnormality Associated with r[i(8)(q10)] in T-Prolymphocytic Leukemia Studied by Classic Cytogenetics and Spectral Karyotype.

Fábio Morato de Oliveira, André F. Marinato, Rafael H. Jácomo, Edgar G. Rizzatti, Roberto P. Falcão, Eduardo M. Rego, Luiz G. Tone, Belinda P. Simões

Blood (2005) 106 (11): 4534.

https://doi.org/10.1182/blood.V106.11.4534.4534

Published: 2005

Journal Articles

BCR/ABL Expression Increases the Formation of Chromosomal Translocations after DNA Damage.

Jamil Dierov, Ph.D., Hesed Padilla-Nash, Ph.D., Thomas Ried, M.D., Ph.D., Martin Carroll, M.D.

Blood (2004) 104 (11): 713.

https://doi.org/10.1182/blood.V104.11.713.713

Published: 2004

Journal Articles

17p Deletion in Acute Myeloid Leukemia and Myelodysplastic Syndrome. Analysis of Breakpoints and Deleted Segments by Fluorescence In Situ

Valérie Soenen, Claude Preudhomme, Christophe Roumier, Agnès Daudignon, Jean Luc Laı̈, Pierre Fenaux

Blood (1998) 91 (3): 1008–1015.

https://doi.org/10.1182/blood.V91.3.1008

Published: 1998

NARROW

Clinical and Cytogenomic Features of Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 (iAMP21) in the Context of Constitutional Ring Chromosome 21

Constitutional Ring Chromosome 21 Predisposes to Acute Lymphoblastic Leukaemia (ALL) with iAMP21

Patient Characteristics and Early Death Predictors in Acute Promyelocytic Leukaemia Patients; Experience from United Arab Emirates (UAE)

Prognostic Impact Of a Newly Defined Structurally Complex Karyotype In Patients With AML and MDS After Allogeneic Stem Cell Transplantation

Gene Amplifications In 84 Patients With Acute Myeloid Leukemia and 31 Patients With Myelodysplastic Syndrome Investigated By Array CGH

Monosomal Karyotype Is Associated With Worse Survival Independent Of Complex Karyotype In Patients With Myelodysplastic Syndrome

RUNX1 Deletions Are a Novel Mechanism of Loss of Function in AML and Are Associated with Adverse Cytogenetics.

Intrachromosomal Amplification of Chromosome 21(iAMP21): Cytogenetic Characterisation and Outcome in Childhood B-Cell Precursor Acute Lymphoblastic Leukaemia (BCP-ALL). A Study On Behalf of the Ponte Di Legno International Childhood ALL Workshop

Thrombocytopenia and Platelet Ultra-Structural Abnormalities Associated with RUNX1 Haploinsufficiency in Monosomy 21 Mosaicism.

SNP-A Karyotyping Provides Clinically Relevant Results In Myeloid Hematologic Disorders with Unsuccessful Routine Cytogenetic Testing.

Atypical Cytogenetic Findings Detected by Whole Genomic Microarray Analysis In Pediatric Acute Lymphoblastic Leukemia Cases

Acute Lymphoblastic Leukemia in a Case of Ring Chromosome

Genome Complexity in Patients with Acute Lymphoblastic Leukaemia Revealed by Array-Based Comparative Genomic Hybridization.

Cytogenetic Classification of T Lineage Acute Lymphoblastic Leukaemia: Multiple Partners of BCL11B and Other Novel Rearrangements.

Translocation t(Y;14)(q12;q11): A New Abnormality Associated with r[i(8)(q10)] in T-Prolymphocytic Leukemia Studied by Classic Cytogenetics and Spectral Karyotype.

BCR/ABL Expression Increases the Formation of Chromosomal Translocations after DNA Damage.

17p Deletion in Acute Myeloid Leukemia and Myelodysplastic Syndrome. Analysis of Breakpoints and Deleted Segments by Fluorescence In Situ

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American Society of Hematology

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American Society of Hematology

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