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Amendments and Corrections | 10 September 2008
Erratum: Inv(11)(q21q23) fuses MLL to the Notch co-activator mastermind-like 2 in secondary T-cell acute lymphoblastic leukemia
- M Metzler
- , M S Staege
- , L Harder
- , D Mendelova
- , J Zuna
- , E Fronkova
- , C Meyer
- , T Flohr
- , D Bednarova
- , J Harbott
- , T Langer
- , S Gesk
- , J Trka
- , R Siebert
- , T Dingermann
- , R Marschalek
- , C Niemeyer
- & W Rascher
Leukemia 22 , 1812–1812

Rights & permissionsfor article Erratum: Inv(11)(q21q23) fuses MLL to the Notch co-activator mastermind-like 2 in secondary T-cell acute lymphoblastic leukemia . Opens in a new window.
31 May 2011
A novel ABL1 fusion to the SH2 containing inositol phosphatase-1 (SHIP1) in acute lymphoblastic leukemia (ALL)
- P M Kakadia
- , B Tizazu
- , G Mellert
- , J Harbott
- , S Röttgers
- , H Quentmeier
- , K Spiekermann
- & S K Bohlander
Leukemia 25 , 1645–1649

Rights & permissionsfor article A novel ABL1 fusion to the SH2 containing inositol phosphatase-1 (SHIP1) in acute lymphoblastic leukemia (ALL) . Opens in a new window.
8 April 2003
Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements
- C-H Pui
- , J M Chessells
- , B Camitta
- , A Baruchel
- , A Biondi
- , J M Boyett
- , A Carroll
- , O B Eden
- , W E Evans
- , H Gadner
- , J Harbott
- , D O Harms
- , C J Harrison
- , P L Harrison
- , N Heerema
- , G Janka-Schaub
- , W Kamps
- , G Masera
- , J Pullen
- , S C Raimondi
- , S Richards
- , H Riehm
- , S Sallan
- , H Sather
- , J Shuster
- , L B Silverman
- , M G Valsecchi
- , E Vilmer
- , Y Zhou
- , P S Gaynon
- & M Schrappe
Leukemia 17 , 700–706

Rights & permissionsfor article Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements . Opens in a new window.
Research | 1 June 2006
Loss of heterozygosity on chromosome 6q14–q24 is associated with poor outcome in children and adolescents with T-cell lymphoblastic lymphoma
- B Burkhardt
- , J Bruch
- , M Zimmermann
- , K Strauch
- , R Parwaresch
- , W-D Ludwig
- , L Harder
- , B Schlegelberger
- , F Mueller
- , J Harbott
- & A Reiter
Leukemia 20 , 1422–1429

Rights & permissionsfor article Loss of heterozygosity on chromosome 6q14–q24 is associated with poor outcome in children and adolescents with T-cell lymphoblastic lymphoma . Opens in a new window.
29 May 1998
A new fingerprint method for sequence analysis of chromosomal translocations at the genomic DNA level
- T Leis
- , R Repp
- , A Borkhardt
- , M Metzler
- , F Schläger
- , J Harbott
- & F Lampert
Leukemia 12 , 758–763

Rights & permissionsfor article A new fingerprint method for sequence analysis of chromosomal translocations at the genomic DNA level . Opens in a new window.
30 April 1998
Detection of hyperdiploid karyotypes (>50 chromosomes) in childhood acute lymphoblastic leukemia (ALL) using fluorescence in situ hybridization (FISH)
- J Ritterbach
- , W Hiddemann
- , JD Beck
- , M Schrappe
- , G Janka-Schaub
- , W-D Ludwig
- , J Harbott
- & F Lampert
Leukemia 12 , 427–433

Rights & permissionsfor article Detection of hyperdiploid karyotypes (>50 chromosomes) in childhood acute lymphoblastic leukemia (ALL) using fluorescence in situ hybridization (FISH) . Opens in a new window.
29 April 2010
ALK fusion genes in children with atypical myeloproliferative leukemia
- S Röttgers
- , M Gombert
- , A Teigler-Schlegel
- , K Busch
- , U Gamerdinger
- , R Slany
- , J Harbott
- & A Borkhardt
Leukemia 24 , 1197–1200

Rights & permissionsfor article ALK fusion genes in children with atypical myeloproliferative leukemia . Opens in a new window.
29 May 1998
Hematological malignancies with a deletion of 11q23: cytogenetic and clinical aspects
- J Harbott
- , M Mancini
- , Ch Verellen-Dumoulin
- , AV Moorman
- & LM Secker-Walker
Leukemia 12 , 823–827

Rights & permissionsfor article Hematological malignancies with a deletion of 11q23: cytogenetic and clinical aspects . Opens in a new window.
Correspondence | 26 May 2005
Acute megakaryoblastic leukemia in children and adolescents, excluding Down's syndrome: improved outcome with intensified induction treatment
- D Reinhardt
- , S Diekamp
- , C Langebrake
- , J Ritter
- , J Stary
- , M Dworzak
- , A Schrauder
- , M Zimmermann
- , G Fleischhack
- , W-D Ludwig
- , J Harbott
- & U Creutzig
Leukemia 19 , 1495–1496

Rights & permissionsfor article Acute megakaryoblastic leukemia in children and adolescents, excluding Down's syndrome: improved outcome with intensified induction treatment . Opens in a new window.
Research | 16 March 2006
Unsupervised proteome analysis of human leukaemia cells identifies the Valosin-containing protein as a putative marker for glucocorticoid resistance
- M Lauten
- , A Schrauder
- , C Kardinal
- , J Harbott
- , K Welte
- , B Schlegelberger
- , M Schrappe
- & N von Neuhoff
Leukemia 20 , 820–826

Rights & permissionsfor article Unsupervised proteome analysis of human leukaemia cells identifies the Valosin-containing protein as a putative marker for glucocorticoid resistance . Opens in a new window.
Correspondence | 6 January 2000
Nineteen cases of the t(1;22)(p13;q13) acute megakaryblastic leukaemia of infants/children and a review of 39 cases: report from a t(1;22) study group
- J Bernstein
- , N Dastugue
- , OA Haas
- , J Harbott
- , NA Heere
- , JL Huret
- , J Landman-Parker
- , MM LeBeau
- , C Leonard
- , G Mann
- , MP Pages
- , C Perot
- , H Pirc-Danoewinata
- , B Roitzheim
- , CM Rubin
- , M Slociak
- & F Viguie
Leukemia 14 , 216–218

Rights & permissionsfor article Nineteen cases of the t(1;22)(p13;q13) acute megakaryblastic leukaemia of infants/children and a review of 39 cases: report from a t(1;22) study group . Opens in a new window.
Correspondence | 5 May 2005
Treatment of relapsed acute myelogeneous leukaemia with MLL/AF6 fusion after stem cell transplantation by intensive reinduction followed by adoptive immunotherapy
- F R Schuster
- , M Führer
- , W Woessmann
- , A Reiter
- , J Harbott
- , S Viehmann
- & A Borkhardt
Leukemia 19 , 1273–1274

Rights & permissionsfor article Treatment of relapsed acute myelogeneous leukaemia with MLL/AF6 fusion after stem cell transplantation by intensive reinduction followed by adoptive immunotherapy . Opens in a new window.
11 April 2001
Treatment response and residual-disease monitoring in initial and relapsed TEL-AML1 positive childhood ALL
- K Seeger
- , S Viehmann
- , D Buchwald
- , J Harbott
- , M Schrappe
- , J Stary
- , G Henze
- & J Trka
Leukemia 15 , 280–282

Rights & permissionsfor article Treatment response and residual-disease monitoring in initial and relapsed TEL-AML1 positive childhood ALL . Opens in a new window.
1 July 2010
Expression of cell–cell interacting genes distinguishes HLXB9/TEL from MLL-positive childhood acute myeloid leukemia
- S Wildenhain
- , C Ruckert
- , S Röttgers
- , J Harbott
- , W-D Ludwig
- , F R Schuster
- , K Beldjord
- , V Binder
- , R Slany
- , J Hauer
- & A Borkhardt
Leukemia 24 , 1657–1660

Rights & permissionsfor article Expression of cell–cell interacting genes distinguishes HLXB9/TEL from MLL-positive childhood acute myeloid leukemia . Opens in a new window.
12 February 2009
Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias
- E Ballabio
- , C D Cantarella
- , C Federico
- , P Di Mare
- , G Hall
- , J Harbott
- , J Hughes
- , S Saccone
- & S Tosi
Leukemia 23 , 1179–1182

Rights & permissionsfor article Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias . Opens in a new window.
13 March 2008
Inv(11)(q21q23) fuses MLL to the Notch co-activator mastermind-like 2 in secondary T-cell acute lymphoblastic leukemia
- M Metzler
- , M S Staege
- , L Harder
- , D Mendelova
- , J Zuna
- , E Fronkova
- , C Meyer
- , T Flohr
- , D Bednarova
- , J Harbott
- , T Langer
- , S Gesk
- , J Trka
- , R Siebert
- , T Dingermann
- , R Marschalek
- , C Niemeyer
- & W Rascher
Leukemia 22 , 1807–1811

Rights & permissionsfor article Inv(11)(q21q23) fuses MLL to the Notch co-activator mastermind-like 2 in secondary T-cell acute lymphoblastic leukemia . Opens in a new window.
30 August 2002
Infant acute lymphoblastic leukemia – combined cytogenetic, immunophenotypical and molecular analysis of 77 cases
- A Borkhardt
- , C Wuchter
- , S Viehmann
- , S Pils
- , A Teigler-Schlegel
- , M Stanulla
- , M Zimmermann
- , W-D Ludwig
- , G Janka-Schaub
- , M Schrappe
- & J Harbott
Leukemia 16 , 1685–1690

Rights & permissionsfor article Infant acute lymphoblastic leukemia – combined cytogenetic, immunophenotypical and molecular analysis of 77 cases . Opens in a new window.
29 May 1998
Down’s syndrome in childhood acute lymphoblastic leukemia: clinical characteristics and treatment outcome in four consecutive BFM trials
- M Dördelmann
- , M Schrappe
- , A Reiter
- , M Zimmermann
- , N Graf
- , G Schott
- , F Lampert
- , J Harbott
- , C Niemeyer
- , J Ritter
- , W Dörffel
- , G Neßler
- , J Kühl
- & H Riehm
Leukemia 12 , 645–651

Rights & permissionsfor article Down’s syndrome in childhood acute lymphoblastic leukemia: clinical characteristics and treatment outcome in four consecutive BFM trials . Opens in a new window.
Correspondence | 25 January 2000
Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life
- M Stanulla
- , B Kasper
- , M Schrappe
- , S Viehmann
- , J Harbott
- , W-D Ludwig
- & K Welte
Leukemia 14 , 337–338

Rights & permissionsfor article Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life . Opens in a new window.
23 May 2003
Monitoring of minimal residual disease (MRD) by real-time quantitative reverse transcription PCR (RQ-RT-PCR) in childhood acute myeloid leukemia with AML1/ETO rearrangement
- S Viehmann
- , A Teigler-Schlegel
- , J Bruch
- , C Langebrake
- , D Reinhardt
- & J Harbott
Leukemia 17 , 1130–1136

Rights & permissionsfor article Monitoring of minimal residual disease (MRD) by real-time quantitative reverse transcription PCR (RQ-RT-PCR) in childhood acute myeloid leukemia with AML1/ETO rearrangement . Opens in a new window.
3 March 2005
No prognostic effect of additional chromosomal abnormalities in children with acute lymphoblastic leukemia and 11q23 abnormalities
- A V Moorman
- , S C Raimondi
- , C-H Pui
- , A Baruchel
- , A Biondi
- , A J Carroll
- , E Forestier
- , P S Gaynon
- , J Harbott
- , D O Harms
- , N Heerema
- , R Pieters
- , M Schrappe
- , L B Silverman
- , E Vilmer
- & C J Harrison
Leukemia 19 , 557–563

Rights & permissionsfor article No prognostic effect of additional chromosomal abnormalities in children with acute lymphoblastic leukemia and 11q23 abnormalities . Opens in a new window.
17 July 2000
Detection of acute leukemia cells with mixed lineage leukemia (MLL) gene rearrangements by flow cytometry using monoclonal antibody 7.1
- C Wuchter
- , J Harbott
- , C Schoch
- , S Schnittger
- , A Borkhardt
- , L Karawajew
- , R Ratei
- , V Ruppert
- , T Haferlach
- , U Creutzig
- , B Dörken
- & W-D Ludwig
Leukemia 14 , 1232–1238

Rights & permissionsfor article Detection of acute leukemia cells with mixed lineage leukemia (MLL) gene rearrangements by flow cytometry using monoclonal antibody 7.1 . Opens in a new window.
Correspondence | 30 September 2004
The GSTT1 deletion polymorphism is associated with initial response to glucocorticoids in childhood acute lymphoblastic leukemia
- B Meissner
- , M Stanulla
- , W-D Ludwig
- , J Harbott
- , A Möricke
- , K Welte
- & M Schrappe
Leukemia 18 , 1920–1923

Rights & permissionsfor article The GSTT1 deletion polymorphism is associated with initial response to glucocorticoids in childhood acute lymphoblastic leukemia . Opens in a new window.
21 October 2004
The International Prognostic Scoring System (IPSS) for childhood myelodysplastic syndrome (MDS) and juvenile myelomonocytic leukemia (JMML)
- H Hasle
- , I Baumann
- , E Bergsträsser
- , S Fenu
- , A Fischer
- , G Kardos
- , G Kerndrup
- , F Locatelli
- , T Rogge
- , K R Schultz
- , J Starý
- , M Trebo
- , M M van den Heuvel-Eibrink
- , J Harbott
- , P Nöllke
- & C M Niemeyer
Leukemia 18 , 2008–2014

Rights & permissionsfor article The International Prognostic Scoring System (IPSS) for childhood myelodysplastic syndrome (MDS) and juvenile myelomonocytic leukemia (JMML) . Opens in a new window.
Research | 29 October 2013
An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome
- C J Harrison
- , A V Moorman
- , C Schwab
- , A J Carroll
- , E A Raetz
- , M Devidas
- , S Strehl
- , K Nebral
- , J Harbott
- , A Teigler-Schlegel
- , M Zimmerman
- , N Dastuge
- , A Baruchel
- , J Soulier
- , M-F Auclerc
- , A Attarbaschi
- , G Mann
- , B Stark
- , G Cazzaniga
- , L Chilton
- , P Vandenberghe
- , E Forestier
- , I Haltrich
- , S C Raimondi
- , M Parihar
- , J-P Bourquin
- , J Tchinda
- , C Haferlach
- , A Vora
- , S P Hunger
- , N A Heerema
- & O A Haas
Leukemia 28 , 1015–1021

Rights & permissionsfor article An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome . Opens in a new window.
Research | 11 October 2013 | Open
The impact of TEL-AML1 (ETV6-RUNX1) expression in precursor B cells and implications for leukaemia using three different genome-wide screening methods
- Y Linka
- , S Ginzel
- , M Krüger
- , A Novosel
- , M Gombert
- , E Kremmer
- , J Harbott
- , R Thiele
- , A Borkhardt
- & P Landgraf
Blood Cancer Journal 3 , e151–e151

Rights & permissionsfor article The impact of TEL-AML1 (ETV6-RUNX1) expression in precursor B cells and implications for leukaemia using three different genome-wide screening methods . Opens in a new window.
Research | 31 May 2007
Identification of two distinct MYC breakpoint clusters and their association with various IGH breakpoint regions in the t(8;14) translocations in sporadic Burkitt-lymphoma
- K Busch
- , T Keller
- , U Fuchs
- , R-F Yeh
- , J Harbott
- , I Klose
- , J Wiemels
- , A Novosel
- , A Reiter
- & A Borkhardt
Leukemia 21 , 1739–1751

Rights & permissionsfor article Identification of two distinct MYC breakpoint clusters and their association with various IGH breakpoint regions in the t(8;14) translocations in sporadic Burkitt-lymphoma . Opens in a new window.
10 March 1999
Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7
- H Hasle
- , M Aricò
- , G Basso
- , A Biondi
- , A Cantù Rajnoldi
- , U Creutzig
- , S Fenu
- , C Fonatsch
- , OA Haas
- , J Harbott
- , G Kardos
- , G Kerndrup
- , G Mann
- , CM Niemeyer
- , H Ptoszkova
- , J Ritter
- , R Slater
- , J Starý
- , B Stollmann-Gibbels
- , AM Testi
- , ER van Wering
- & M Zimmermann
Leukemia 13 , 376–385

Rights & permissionsfor article Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7 . Opens in a new window.
10 December 2009
Long-term results of five consecutive trials in childhood acute lymphoblastic leukemia performed by the ALL-BFM study group from 1981 to 2000
- A Möricke
- , M Zimmermann
- , A Reiter
- , G Henze
- , A Schrauder
- , H Gadner
- , W D Ludwig
- , J Ritter
- , J Harbott
- , G Mann
- , T Klingebiel
- , F Zintl
- , C Niemeyer
- , B Kremens
- , F Niggli
- , D Niethammer
- , K Welte
- , M Stanulla
- , E Odenwald
- , H Riehm
- & M Schrappe
Leukemia 24 , 265–284

Rights & permissionsfor article Long-term results of five consecutive trials in childhood acute lymphoblastic leukemia performed by the ALL-BFM study group from 1981 to 2000 . Opens in a new window.
Research | 20 November 2008
Favorable prognostic impact of NPM1 gene mutations in childhood acute myeloid leukemia, with emphasis on cytogenetically normal AML
- I H I M Hollink
- , C M Zwaan
- , M Zimmermann
- , T C J M Arentsen-Peters
- , R Pieters
- , J Cloos
- , G J L Kaspers
- , S S N de Graaf
- , J Harbott
- , U Creutzig
- , D Reinhardt
- , M M van den Heuvel-Eibrink
- & C Thiede
Leukemia 23 , 262–270

Rights & permissionsfor article Favorable prognostic impact of NPM1 gene mutations in childhood acute myeloid leukemia, with emphasis on cytogenetically normal AML . Opens in a new window.
8 January 2004
In vitro drug-resistance profile in infant acute lymphoblastic leukemia in relation to age, MLL rearrangements and immunophenotype
- N L Ramakers-van Woerden
- , H B Beverloo
- , A J P Veerman
- , B M Camitta
- , A H Loonen
- , E R van Wering
- , R M Slater
- , J Harbott
- , M L den Boer
- , W D Ludwig
- , O A Haas
- , G E Janka-Schaub
- & R Pieters
Leukemia 18 , 521–529

Rights & permissionsfor article In vitro drug-resistance profile in infant acute lymphoblastic leukemia in relation to age, MLL rearrangements and immunophenotype . Opens in a new window.
26 March 2004
Secondary cytogenetic aberrations in childhood Philadelphia chromosome positive acute lymphoblastic leukemia are nonrandom and may be associated with outcome
- N A Heerema
- , J Harbott
- , S Galimberti
- , B M Camitta
- , P S Gaynon
- , G Janka-Schaub
- , W Kamps
- , G Basso
- , C-H Pui
- , M Schrappe
- , M-F Auclerc
- , A J Carroll
- , V Conter
- , C J Harrison
- , J Pullen
- , S C Raimondi
- , S Richards
- , H Riehm
- , H N Sather
- , J J Shuster
- , L B Silverman
- , M G Valsecchi
- & M Aricò
Leukemia 18 , 693–702

Rights & permissionsfor article Secondary cytogenetic aberrations in childhood Philadelphia chromosome positive acute lymphoblastic leukemia are nonrandom and may be associated with outcome . Opens in a new window.
20 December 2000
Long-term results of four consecutive trials in childhood ALL performed by the ALL-BFM study group from 1981 to 1995
- M Schrappe
- , A Reiter
- , M Zimmermann
- , J Harbott
- , W-D Ludwig
- , G Henze
- , H Gadner
- , E Odenwald
- & H Riehm
Leukemia 14 , 2205–2222

Rights & permissionsfor article Long-term results of four consecutive trials in childhood ALL performed by the ALL-BFM study group from 1981 to 1995 . Opens in a new window.
Research | 5 March 2009
New insights to the MLL recombinome of acute leukemias
- C Meyer
- , E Kowarz
- , J Hofmann
- , A Renneville
- , J Zuna
- , J Trka
- , R Ben Abdelali
- , E Macintyre
- , E De Braekeleer
- , M De Braekeleer
- , E Delabesse
- , M P de Oliveira
- , H Cavé
- , E Clappier
- , J J M van Dongen
- , B V Balgobind
- , M M van den Heuvel-Eibrink
- , H B Beverloo
- , R Panzer-Grümayer
- , A Teigler-Schlegel
- , J Harbott
- , E Kjeldsen
- , S Schnittger
- , U Koehl
- , B Gruhn
- , O Heidenreich
- , L C Chan
- , S F Yip
- , M Krzywinski
- , C Eckert
- , A Möricke
- , M Schrappe
- , C N Alonso
- , B W Schäfer
- , J Krauter
- , D A Lee
- , U zur Stadt
- , G Te Kronnie
- , R Sutton
- , S Izraeli
- , L Trakhtenbrot
- , L Lo Nigro
- , G Tsaur
- , L Fechina
- , T Szczepanski
- , S Strehl
- , D Ilencikova
- , M Molkentin
- , T Burmeister
- , T Dingermann
- , T Klingebiel
- & R Marschalek
Leukemia 23 , 1490–1499

Rights & permissionsfor article New insights to the MLL recombinome of acute leukemias . Opens in a new window.

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Erratum: Inv(11)(q21q23) fuses MLL to the Notch co-activator mastermind-like 2 in secondary T-cell acute lymphoblastic leukemia

A novel ABL1 fusion to the SH2 containing inositol phosphatase-1 (SHIP1) in acute lymphoblastic leukemia (ALL)

Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements

Loss of heterozygosity on chromosome 6q14–q24 is associated with poor outcome in children and adolescents with T-cell lymphoblastic lymphoma

A new fingerprint method for sequence analysis of chromosomal translocations at the genomic DNA level

Detection of hyperdiploid karyotypes (>50 chromosomes) in childhood acute lymphoblastic leukemia (ALL) using fluorescence in situ hybridization (FISH)

ALK fusion genes in children with atypical myeloproliferative leukemia

Hematological malignancies with a deletion of 11q23: cytogenetic and clinical aspects

Acute megakaryoblastic leukemia in children and adolescents, excluding Down's syndrome: improved outcome with intensified induction treatment

Unsupervised proteome analysis of human leukaemia cells identifies the Valosin-containing protein as a putative marker for glucocorticoid resistance

Nineteen cases of the t(1;22)(p13;q13) acute megakaryblastic leukaemia of infants/children and a review of 39 cases: report from a t(1;22) study group

Treatment of relapsed acute myelogeneous leukaemia with MLL/AF6 fusion after stem cell transplantation by intensive reinduction followed by adoptive immunotherapy

Treatment response and residual-disease monitoring in initial and relapsed TEL-AML1 positive childhood ALL

Expression of cell–cell interacting genes distinguishes HLXB9/TEL from MLL-positive childhood acute myeloid leukemia

Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias

Inv(11)(q21q23) fuses MLL to the Notch co-activator mastermind-like 2 in secondary T-cell acute lymphoblastic leukemia

Infant acute lymphoblastic leukemia – combined cytogenetic, immunophenotypical and molecular analysis of 77 cases

Down’s syndrome in childhood acute lymphoblastic leukemia: clinical characteristics and treatment outcome in four consecutive BFM trials

Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life

Monitoring of minimal residual disease (MRD) by real-time quantitative reverse transcription PCR (RQ-RT-PCR) in childhood acute myeloid leukemia with AML1/ETO rearrangement

No prognostic effect of additional chromosomal abnormalities in children with acute lymphoblastic leukemia and 11q23 abnormalities

Detection of acute leukemia cells with mixed lineage leukemia (MLL) gene rearrangements by flow cytometry using monoclonal antibody 7.1

The GSTT1 deletion polymorphism is associated with initial response to glucocorticoids in childhood acute lymphoblastic leukemia

The International Prognostic Scoring System (IPSS) for childhood myelodysplastic syndrome (MDS) and juvenile myelomonocytic leukemia (JMML)

An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome

The impact of TEL-AML1 (ETV6-RUNX1) expression in precursor B cells and implications for leukaemia using three different genome-wide screening methods

Identification of two distinct MYC breakpoint clusters and their association with various IGH breakpoint regions in the t(8;14) translocations in sporadic Burkitt-lymphoma

Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7

Long-term results of five consecutive trials in childhood acute lymphoblastic leukemia performed by the ALL-BFM study group from 1981 to 2000

Favorable prognostic impact of NPM1 gene mutations in childhood acute myeloid leukemia, with emphasis on cytogenetically normal AML

In vitro drug-resistance profile in infant acute lymphoblastic leukemia in relation to age, MLL rearrangements and immunophenotype

Secondary cytogenetic aberrations in childhood Philadelphia chromosome positive acute lymphoblastic leukemia are nonrandom and may be associated with outcome

Long-term results of four consecutive trials in childhood ALL performed by the ALL-BFM study group from 1981 to 1995

New insights to the MLL recombinome of acute leukemias

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