MLPA as a complementary tool for diagnosis of chromosome 21 aberrations in childhood BCP-ALL
Author:
Funder
National Science Centre
National Center of Research and Development
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s13353-019-00509-8.pdf
Reference26 articles.
1. Benard-Slagter A et al (2017) Digital multiplex ligation-dependent probe amplification for detection of key copy number alterations in T- and B-cell lymphoblastic leukemia. J Mol Diagn Am Soc Invest Pathol Assoc Mol Pathol 19(5):659–672. https://doi.org/10.1016/j.jmoldx.2017.05.004
2. Brown A et al (2007) Characterization of high-hyperdiploidy in childhood acute lymphoblastic leukemia with gain of a single chromosome 21. Leuk Lymphoma 48(12):2457–2460. https://doi.org/10.1080/10428190701656110
3. Depil S et al (1998) Amplification of band q22 of chromosome 21, including AML1, in older children with acute lymphoblastic leukemia: an emerging molecular cytogenetic subgroup. Leukemia. https://doi.org/10.1038/sj.leu.2403000
4. Duployez N et al (2015) Diagnosis of intrachromosomal amplification of chromosome 21 (iAMP21) by molecular cytogenetics in pediatric acute lymphoblastic leukemia. Clinical Case Reports 3(10):814–816. https://doi.org/10.1002/ccr3.357
5. Fuka G et al (2015) Evaluation of multiplex ligation dependent probe amplification (MLPA) for identification of acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21 (iAMP21) in a Brazilian population. Mol Cytogenet 8(1). https://doi.org/10.1186/s13039-015-0147-2
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3. Integrating copy number data of 64 iAMP21 BCP-ALL patients narrows the common region of amplification to 1.57 Mb;Frontiers in Oncology;2023-02-23
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