Wikidata

(Q71020950)

English

TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis

scientific article published on 01 December 1995

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Statements

title
TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8609706
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8609706%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
author name string

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