1. Corona-Rivera A, Bobadilla-Morales L, Cruz-Osorio RM, et al. Translocation t (5; 15)(q15;
q11-13) infant case with acute lymphoblastic leukemia and literature review: prognosis …

Studies evaluating clinical characteristics and potential risk factors associated with outcome
in pediatric patients with acute myeloid leukemia (AML) harboring t (16; 16)(p13. 1; …

Aim: The translocation (6; 9)(p23; q34) is a rare cytogenetic aberration found in patients with
acute myeloid leukemia (AML)(about 1% of all AML), and correlates with poor clinical …

We report the nonrandom occurrence and frequency of the t (1; 22)(p13; q13) in acute
myeloid leukemia (AML) and its close association with the French-American-British M7 …

The t (9; 11)(p21; q23) has been associated with characteristic clinical features and a
superior treatment outcome in previously untreated pediatric acute myeloblastic leukemia …

Infant acute lymphoblastic leukemia (IALL), which occurs within the first 12 months of life,
clinically tends to have hepatosplenomegaly, leukocytosis, central nervous system …

Acute myeloid leukaemia (AML) is characterised by distinct nonrandom karyotypic changes
that in many cases have been recognised to represent one of the initial pathogenic changes …

The t (4; 12)(q12; p13) in acute myeloid leukemia (AML) is a rare finding with less than 30
cases described in the literature. The few cases reported show that this subtype of AML …

[Considerations on a case of acute leukemia with neurological manifestations & rare
osseous localizations]. - Abstract - Europe PMC Sign in | Create an account https://orcid.org …

A 29-year-old woman having acute myelogeneous leukemia-M1 subtype with the
chromosomal abnormality t (16; 21)(p11; q22) is presented. Complete blood count at onset …