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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Appl Genet
Autors principals: Wrona, Ewa, Braun, Marcin, Pastorczak, Agata, Taha, Joanna, Lejman, Monika, Kowalczyk, Jerzy, Fendler, Wojciech, Młynarski, Wojciech
Format: Artigo
Idioma:Inglês
Publicat: Springer Berlin Heidelberg 2019
Matèries:
Human Genetics • Original Paper
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6803575/
https://ncbi.nlm.nih.gov/pubmed/31456164
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13353-019-00509-8
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars