MLPA as a complementary tool for diagnosis of chromosome 21 aberrations in childhood BCP-ALL

Chromosome 21 abnormalities are the most frequent genetic findings in childhood B cell precursor acute lymphoblastic leukemia (BCP-ALL) cases. Majority of patients are effectively diagnosed with fluorescence in situ hybridization (FISH) and karyotyping; however, some cases may require additional too...

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Detalles Bibliográficos
Autores principales: Wrona, Ewa, Braun, Marcin, Pastorczak, Agata, Taha, Joanna, Lejman, Monika, Kowalczyk, Jerzy, Fendler, Wojciech, Młynarski, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Human Genetics • Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803575/
https://www.ncbi.nlm.nih.gov/pubmed/31456164
http://dx.doi.org/10.1007/s13353-019-00509-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803575/
https://www.ncbi.nlm.nih.gov/pubmed/31456164
http://dx.doi.org/10.1007/s13353-019-00509-8

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