References

Altshuler, D., L. Brooks, A. Chakravarti, F. Collins, M. Daly and P. Donnelly, 2005. A haplotype map of the human genome. Nature, 437: 1299-1320.

American Society of Clinical Oncology, 2010. Nucleotide polymorphism in the mutational hotspot of wt1 predicts a favorable outcome in patients with cytogenetically normal acute myeloid leukemia. JCO 570-577.

Aplenc, R. and B. Lange, 2004. Pharmacogenetic determinants of outcome in acute lymphoblastic leukaemia. Br. J. Haematol., 125: 421-434.
PubMed  |  

Bennett, J.H., 1845. Case of hypertrophy of the spleen and liver, in which death took place from suppuration of the blood. Edinburgh Med. Surg. J., 64: 413-423.

Bennett, J.H., 1845. Leukemia was first reported. The European Hematology Association 2, 1 1466-4860.

Cargill, M., D. Altshuler, J. Ireland, P. Sklar and K. Ardlie et al., 1999. Characterization of singlenucleotidepolymorphisms in coding regions of human genes. Nat. Genet., 22: 231-238.
PubMed  |  

Carlson, C.S., M.A. Eberle, M.J. Rieder, J.D. Smith, L. Kruglyak and D.A. Nickerson, 2003. Additional SNPS and Linkage-disequilibrium analyses are necessary for 521, Whole-genome association studies in humans. Nat. Genet., 33: 518-521.
CrossRef  |  

Cgry, L., D.A. Campbell and N.K. Spur, 2000. Single nucleotide polymorphisms as a tools in human genetics. Hum. Mol. Gene., 9: 2403-2408.

Collins, F.S., M.S. Guyer and A. Chakravarti, 1997. Variations on atheme: Cataloging human DNA sequence variations. Science, 278: 1580-1581.
CrossRef  |  

Cooper, D.N. and H. Youssoufian, 1988. The CpG dinucleotide andhuman genetic disease. Hum. Genet., 78: 151-155.
PubMed  |  

Cooper, D.N. and M. Krawczak, 1990. The mutational spectrum of single base-pair substitutions causing human genetic disease: Patterns and predictions. Hum. Genet., 85: 55-74.
CrossRef  |  Direct Link  |  

Damm, F., M. Heuser, M. Morgan, H. Yun and A. Grobhennig et al., 2010. Single nucleotide polymorphism in the mutational hotspot of WT1 predicts a favorable outcome in patients with cytogenetically a normal acute myeloid leukemia. J. Clin. Oncol., 28: 578-585.
CrossRef  |  

Erichsen, H.C. and S.J. Chanock, 2004. SNPs in cancer research and treatment. Br. J. Cancer, 90: 747-751.
CrossRef  |  

Green, AR., 1992. Transcription factors, translocations and haematological malignancies. Blood Rev., 6: 118-124.
PubMed  |  

Herr, A., R. Grutzmann, A. Matthaei, J. Artelt, E. Schrock, A. Rump and C. Pilarsky, 2005. High-resolution analysis of chromosomal imbalances using the Affymetrix 10K SNP genotyping chip. Genomics, 85: 392-400.
PubMed  |  

Kawamata, N., S. Ogawa, M. Zimmermann, M. Kato and M. Sanada et al., 2008. Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. Blood, 111: 776-784.
CrossRef  |  

Masood, E., 1999. As consortium plans free SNP map of human genome. Nature, 398: 545-546.
PubMed  |  

Mooney, S., 2005. Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis. Brief. Bioinform., 6: 44-56.
CrossRef  |  PubMed  |  Direct Link  |  

Mullighan, C.G., X. Su, J. Ma, W. Yang and M.V. Relling et al., 2007. Genome-wide profiling of high-risk pediatric Acute Lymphoblastic Leukemia (ALL): The ALL pilot project for the Therapeutically Applicable Research To Generate Effective Treatments (TARGET) initiative. Blood ASH Ann. Meeting, 110: 229-229.

Murphy, J.B., 1913. Transplantation of tissue to the embryo of foreign species it bearing on questions of tissue specificity and tumor immunity. J. Exp., 17: 482-493.

Nickerson, D.A., S.L. Taylor, K.M. Weiss, A.G. Clark and R.G. Hutchinson et al., 1998. DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene. Nat. Genet., 19: 233-240.
CrossRef  |  

Pui, C.H., W.M. Crist and A.T. Look, 1990. Biology and clinical significance of cytogenetic abnormalities in childhood acute lymphoblastic leukemia. Blood, 76: 1449-1463.
PubMed  |  

Rabbitts, T.H., 1991. Translocations, master genes and differences between the origins of acute and chronic leukemias. Cell, 67: 641-644.
PubMed  |  

Rowley, J.D., 1990. Molecular cytogenetics: Rosetta stone for understanding cancer-twenty-ninth G.H.A. clowes memorial award lecture. Cancer Res., 50: 3816-3825.
PubMed  |  

Seeker-walker, L.M., S.D. Lawler and R.M. Hardisty, 1978. Prognostic implication of chromosomal finding in acute lymphoblastic leukemia at diagnosis. Br. Med. J., 2: 1529-1530.
Direct Link  |  

Susana, C.R., 1993. Classified all into four subtype. Blood, 81: 2237-2257.

Wang and Scott, 2007. Study assesses leukemia cell DNA obtained from 242 pediatric patients with all through the use of SNP arrays that provide the highest resolution analysis of genomic integrity to data. Gene Dev., 21: 2845-2849.

Wang, D.G., J.B. Fan, C.J. Siao, A. Berno and P. Young et al., 1998. Large-scale identification, mapping and genotyping of single-nucleotide polymorphisms in the human genome. Science, 280: 1077-1082.
PubMed  |