A tiling path 33K BAC array was used to study 28 children with acute lymphoblastic leukaemia (ALL) who had normal or failed G-banded karyotypes. Twenty-two patients (79%) had a total of 135 copy number alterations (CNA) (69 gains and 66 losses); most of these patients showed CNA that were below the resolution of G-banding. Molecular cytogenetic and array comparative genomic hybridization results enabled the division of B-precursor ALL patients into five groups: high hyperdiploidy, intrachromosomal amplification of 21q, ETV6/RUNX1 rearrangement, others and no CNA. Apart from a shared deletion of 9p21.3, T-ALL patients had additional small CNA, with no region in common
Chromosomal abnormalities are important for the risk stratification of acute lymphoblastic leukemia/...
P>Metaphase (M-) and array (A-) Comparative Genomic Hybridization (CGH) were used to investigate 40 ...
Background - Many cases of acute lymphoblastic leukemia (ALL) carry visible acquired chromosomal cha...
Acute lymphoblastic leukemia is the most common malignancy in children. The most important examinati...
Chromosomal abnormalities are important for the classification and risk stratification of patients w...
Genetic alterations of the short arm of chromosome 9 are frequent in acute lymphoblastic leukemia. W...
AbstractGenetic alterations of the short arm of chromosome 9 are frequent in acute lymphoblastic leu...
Chromosomal copy number (CN) is an important prognostic index in childhood acute lymphoblastic leuka...
In childhood acute lymphoblastic leukaemia (ALL), cytogenetics plays an essential role in diagnosis ...
Spectral karyotyping (SKY) on metaphase spreads from 15 high hyperdiploid (>51 chromosomes) childhoo...
The dic( 7; 9)( p11 similar to 13; p11 similar to 13) is a recurrent chromosomal abnormality in acut...
Although the dic(9;20)(p11-13;q11) is a recurrent chromosomal abnormality in paediatric B-cell precu...
Background: Acute lymphoblastic leukemia (ALL) is not a single uniform disease. It consists of sever...
The chromosomal translocation t(12;21) resulting in the ETV6/RUNX1 fusion gene is the most frequent ...
Identifying additional genetic alterations associated with poor prognosis in acute lymphoblastic leu...
Chromosomal abnormalities are important for the risk stratification of acute lymphoblastic leukemia/...
P>Metaphase (M-) and array (A-) Comparative Genomic Hybridization (CGH) were used to investigate 40 ...
Background - Many cases of acute lymphoblastic leukemia (ALL) carry visible acquired chromosomal cha...
Acute lymphoblastic leukemia is the most common malignancy in children. The most important examinati...
Chromosomal abnormalities are important for the classification and risk stratification of patients w...
Genetic alterations of the short arm of chromosome 9 are frequent in acute lymphoblastic leukemia. W...
AbstractGenetic alterations of the short arm of chromosome 9 are frequent in acute lymphoblastic leu...
Chromosomal copy number (CN) is an important prognostic index in childhood acute lymphoblastic leuka...
In childhood acute lymphoblastic leukaemia (ALL), cytogenetics plays an essential role in diagnosis ...
Spectral karyotyping (SKY) on metaphase spreads from 15 high hyperdiploid (>51 chromosomes) childhoo...
The dic( 7; 9)( p11 similar to 13; p11 similar to 13) is a recurrent chromosomal abnormality in acut...
Although the dic(9;20)(p11-13;q11) is a recurrent chromosomal abnormality in paediatric B-cell precu...
Background: Acute lymphoblastic leukemia (ALL) is not a single uniform disease. It consists of sever...
The chromosomal translocation t(12;21) resulting in the ETV6/RUNX1 fusion gene is the most frequent ...
Identifying additional genetic alterations associated with poor prognosis in acute lymphoblastic leu...
Chromosomal abnormalities are important for the risk stratification of acute lymphoblastic leukemia/...
P>Metaphase (M-) and array (A-) Comparative Genomic Hybridization (CGH) were used to investigate 40 ...
Background - Many cases of acute lymphoblastic leukemia (ALL) carry visible acquired chromosomal cha...