Related references
Note: Only part of the references are listed.Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays
Go Yamamoto et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression
R. P. Kuiper et al.
LEUKEMIA (2007)
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
Charles G. Mullighan et al.
NATURE (2007)
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
Linda M. Scott et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
Drug therapy - Treatment of acute lymphoblastic leukemia
CH Pui et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia
RL Levine et al.
BLOOD (2005)
A haplotype map of the human genome
D Altshuler et al.
NATURE (2005)
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event
MT Teh et al.
CANCER RESEARCH (2005)
On the road to cancer: Aneuploidy and the mitotic checkpoint
GJPL Kops et al.
NATURE REVIEWS CANCER (2005)
Molecular genetics of acute lymphoblastic leukemia
SA Armstrong et al.
JOURNAL OF CLINICAL ONCOLOGY (2005)
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays
Y Nannya et al.
CANCER RESEARCH (2005)
Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma
LA Garraway et al.
NATURE (2005)
High concordance from independent studies by the Children's Cancer Group (CCG) and Pediatric Oncology Group (POG) associating favorable prognosis with combined trisomies 4, 10, and 17 in children with NCI Standard-Risk B-precursor Acute Lymphoblastic Leukemia: a Children's Oncology Group (COG) initiative
MJ Sutcliffe et al.
LEUKEMIA (2005)
A genome-wide scalable SNP genotyping assay using microarray technology
KL Gunderson et al.
NATURE GENETICS (2005)
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
C James et al.
NATURE (2005)
A gain-of-function mutation of JAK2 in myeloproliferative disorders
R Kralovics et al.
NEW ENGLAND JOURNAL OF MEDICINE (2005)
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
RL Levine et al.
CANCER CELL (2005)
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
EJ Baxter et al.
LANCET (2005)
The V617F mutation in Jak2 is not found in childhood acute lymphoblastic leukaemia
S Sulong et al.
BRITISH JOURNAL OF HAEMATOLOGY (2005)
Mechanisms of disease: Acute lymphoblastic leukemia
C Pui et al.
NEW ENGLAND JOURNAL OF MEDICINE (2004)
Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia
C Graux et al.
NATURE GENETICS (2004)
Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays
H Matsuzaki et al.
NATURE METHODS (2004)
Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements
D Kotzot
JOURNAL OF MEDICAL GENETICS (2001)
Share Paper
