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Expert Review of Molecular Diagnostics Volume 12, 2012 - Issue 3
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Theme: Genetic & Genomics Applications - Review

Detection of copy number alterations in acute myeloid leukemia and myelodysplastic syndromes

Meagan A Jacoby Department of Internal Medicine, Washington University School of Medicine, Division of Oncology, Stem Cell Biology Section, Campus Box 8007, 660 South Euclid Avenue, St Louis, MO 63110, USA
&
Matthew J Walter Department of Internal Medicine, Washington University School of Medicine, Division of Oncology, Stem Cell Biology Section, Campus Box 8007, 660 South Euclid Avenue, St Louis, MO 63110, USA; Siteman Cancer Center, Washington University, St Louis, MO, USA. [email protected]; Department of Genetics, Washington University, St Louis, MO, USA; Siteman Cancer Center, Washington University, St Louis, MO, USA. [email protected]
Pages 253-264 | Published online: 09 Jan 2014

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Katrin Mäbert, Monica Cojoc, Claudia Peitzsch, Ina Kurth, Serhiy Souchelnytskyi & Anna Dubrovska. (2014) Cancer biomarker discovery: Current status and future perspectives. International Journal of Radiation Biology 90:8, pages 659-677.
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Etienne De Braekeleer, Nathalie Douet-Guilbert & Marc De Braekeleer. (2014) Genetic diagnosis in malignant hemopathies: from cytogenetics to next-generation sequencing. Expert Review of Molecular Diagnostics 14:2, pages 127-129.
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Zaher K Otrock, Ramon V Tiu, Jaroslaw P Maciejewski & Mikkael A Sekeres. (2013) The need for additional genetic markers for myelodysplastic syndrome stratification: what does the future hold for prognostication?. Expert Review of Hematology 6:1, pages 59-68.
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Articles from other publishers (15)

Huan Li, Fang Hu, Robert Peter Gale, Mikkael A. Sekeres & Yang Liang. (2022) Myelodysplastic syndromes. Nature Reviews Disease Primers 8:1.
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Man Gao, Shibo Li, Lina Wang, Shu Nie, Hui Pang, Xianglan Lu, Xianfu Wang, Mingwei Wang, Shirong Guo, Yuhan Ma & Fanzheng Meng. (2020) Identification of a cryptic submicroscopic deletion using a combination of fluorescence in situ hybridization and array comparative genomic hybridization in a t(3;5)(q25;q35)-positive acute myeloid leukemia patient. Medicine 99:43, pages e22789.
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Laurène Fenwarth, Nicolas Duployez, Xavier Thomas, Nicolas Boissel, Sandrine Geffroy, Alice Marceau-Renaut, Denis Caillot, Emmanuel Raffoux, Emilie Lemasle, Jean-Pierre Marolleau, Céline Berthon, Meyling H. Cheok, Pauline Peyrouze, Arnaud Pigneux, Norbert Vey, Karine Celli-Lebras, Christine Terré, Claude Preudhomme & Hervé Dombret. (2019) Clofarabine Improves Relapse-Free Survival of Acute Myeloid Leukemia in Younger Adults with Micro-Complex Karyotype. Cancers 12:1, pages 88.
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Kevin E. Fisher, Linsheng Zhang & Charles E. Hill. 2019. Genomic Applications in Pathology. Genomic Applications in Pathology 269 287 .
Rashmi Kanagal-Shamanna, Jennelle C. Hodge, Tracy Tucker, Shashi Shetty, Ashwini Yenamandra, Amanda Dixon-McIver, Christine Bryke, Emma Huxley, Patrick A. Lennon, Gordana Raca, Xinjie Xu, Sally Jeffries, Fabiola Quintero-Rivera, Patricia T. Greipp, Marilyn L. Slovak, M. Anwar Iqbal & Min Fang. (2018) Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms. Cancer Genetics 228-229, pages 197-217.
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Edwige Voisset, Eva MoravcsikEva W. StratfordAmie JayeChristopher J. PalgraveRobert K. HillsPaolo Salomoni, Scott C. Kogan, Ellen SolomonDavid Grimwade. (2018) Pml nuclear body disruption cooperates in APL pathogenesis and impairs DNA damage repair pathways in mice. Blood 131:6, pages 636-648.
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Qibin Song, Min Peng, Yuxin Chu & Shiang Huang. (2017) Techniques for detecting chromosomal aberrations in myelodysplastic syndromes. Oncotarget 8:37, pages 62716-62729.
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Purvi Mohanty, Seema Korgaonkar, Chandrakala Shanmukhaiah, Kanjaksha Ghosh & Babu Rao Vundinti. (2016) Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes. Blood Cells, Molecules, and Diseases 59, pages 52-57.
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Xi Jiang, Chao Hu, Stephen Arnovitz, Jason Bugno, Miao Yu, Zhixiang Zuo, Ping Chen, Hao Huang, Bryan Ulrich, Sandeep Gurbuxani, Hengyou Weng, Jennifer Strong, Yungui Wang, Yuanyuan Li, Justin Salat, Shenglai Li, Abdel G. Elkahloun, Yang Yang, Mary Beth Neilly, Richard A. Larson, Michelle M. Le Beau, Tobias Herold, Stefan K. Bohlander, Paul P. Liu, Jiwang Zhang, Zejuan Li, Chuan He, Jie Jin, Seungpyo Hong & Jianjun Chen. (2016) miR-22 has a potent anti-tumour role with therapeutic potential in acute myeloid leukaemia. Nature Communications 7:1.
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Mohammad Hussaini. (2015) Biomarkers in Hematological Malignancies: A Review of Molecular Testing in Hematopathology. Cancer Control 22:2, pages 158-166.
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Kevin E. Fisher & Charles E. Hill. 2015. Genomic Applications in Pathology. Genomic Applications in Pathology 297 319 .
Renata Lukackova, Maria Gerykova Bujalkova, Lubica Majerova & Beata Mladosievicova. (2014) Molecular genetic methods in the diagnosis of myelodysplastic syndromes. A review. Biomedical Papers 158:3, pages 339-345.
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Susan Mahler Zneimer. 2014. Cytogenetic Abnormalities. Cytogenetic Abnormalities 577 593 .
Mikkael A. Sekeres & Corey Cutler. (2014) How we treat higher-risk myelodysplastic syndromes. Blood 123:6, pages 829-836.
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Hatice Gulcin Ozer, Aisulu Usubalieva, Adrienne DorranceAyse Selen Yilmaz, Michael CaligiuriGuido MarcucciKun Huang. (2015) Identification of Medium-Sized Copy Number Alterations in Whole-Genome Sequencing. Cancer Informatics 13s3, pages CIN.S14023.
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