Microarray, gene sequencing, and reverse transcriptase–polymerase chain reaction analyses of a cryptic PML-RARA translocation

Author:

Koshy Jason,Qian You-Wen,Bhagwath Gayathri,Willis Maurice,Kelley Todd W.,Papenhausen Peter

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference9 articles.

1. Identification of PML/RARA fusion gene transcripts that showed no t(15;17) with conventional karyotyping and fluorescent in situ hybridization;Choughule;Genet Mol Res,2009

2. Arber, D, Vardiman J, editors. Acute promyelocytic leukemia with t(15;17)(q22;q12) PML-RARA. In: Swerdlow S, Campo E, Harris N, editors. WHO classification of tumours of haematopoietic and lymphoid tissues, 4th ed. Geneva: World Health Organization Publications. 2008; pp.112–114.

3. Identification of PML-RARA rearrangement by RT-PCR and sequencing in an acute promyelocytic leukemia without t(15;17) on G-banding and FISH;Han;Leuk Res,2007

4. Use of whole-genome sequencing to diagnose a cryptic fusion oncogene;Welch;JAMA,2011

5. Interstitial insertion of RARA gene into PML gene in a patient with acute promyelocytic leukemia (APL) lacking the classic t(15;17);Goldschmidt;Hematology,2010

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