References
- Luna-Fineman S, Shannon KM, Lange BJ. Childhood mono somy 7: epidemiology, biology and mech-anistic implications. Blood. 1995;85: 1985–1999.
- Mitelman F, ed., ISCN (1995): An International System for Human Cytogenetic Nomenthture. Basel: Karger; 1995.
- Barnard DR, Kalousek DK, Wiersma SR, et al. Morphologic, immunologic, and cytogenetic classi-fication of acute myeloid leukemia and myelodysplastic syndrome in childhood: a report from the Childrens Cancer Group. Leukemia. 1996;10:5–12.
- Martinez-Climent JA, Garcia-Conde J. Chromosomal rearrangements in childhood acute myeloid leukemia and myelodysplastic syndromes. J Pediatr Hematol Oncol. 1999;21:91–102.
- Side L, Taylor B, Cayouette M, et al. Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders. N Eng J Med. 1997336:1713-1720.
- Johnson EJ, Scherer SW, Osborne L, et al. Molecular definition of a narrow interval at 7q22.1 associ-ated with myelodysplasia. Blood. 1996;87:3579–3586.
- Le Beau MM, Espinosa Rill, Davis EM, Eisenbart JD, Larson RA, Green ED. Cytogenetic and molecu-lar delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases. Blood. 199688:1930-1935.
- Pedersen B, Ellegaard J. A factor encoded by 7q31 suppresses expansion of the 7q- clone and delays cytogenetic progression. Cancer Genet Cytogenet. 1994;78:181–188.
- Lubbert M, Mirro J Jr, Kitchingman G, et al. Prevalence of N-Ras mutations in children with myelodys-plastic syndromes and acute myeloid leukemia. Oncogene 1992;7:263–268.
- Kiuru-Kuhlefelt S, Kristo P, Ruutu T, Knuutila S, Kere J. Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm. Leukemia. 1997;11: 2097–2104.