Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture-Reference-Cited by-同舟云学术

Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture

Published:2013-04-18 Issue:9 Volume:27 Page:1820-1825
ISSN:0887-6924
Container-title:Leukemia
language:en
Short-container-title:Leukemia

Author:

Conte N,Varela I,Grove C,Manes N,Yusa K,Moreno T,Segonds-Pichon A,Bench A,Gudgin E,Herman B,Bolli N,Ellis P,Haddad D,Costeas P,Rad R,Scott M,Huntly B,Bradley A,Vassiliou G S

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Link

http://www.nature.com/articles/leu2013117.pdf

Reference24 articles.

1. Stratton MR, Campbell PJ, Futreal PA . The cancer genome. Nature 2009; 458: 719–724.

2. Ley TJ, Mardis ER, Ding L, Fulton B, McLellan MD, Chen K et al. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature 2008; 456: 66–72.

3. Mardis ER, Ding L, Dooling DJ, Larson DE, McLellan MD, Chen K et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med 2009; 361: 1058–1066.

4. Patel JP, Gonen M, Figueroa ME, Fernandez H, Sun Z, Racevskis J et al. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. N Engl J Med 2012; 366: 1079–1089.

5. Grossmann V, Tiacci E, Holmes AB, Kohlmann A, Martelli MP, Kern W et al. Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype. Blood 2011; 118: 6153–6163.

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