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Volumn 180, Issue 2, 2008, Pages 163-164

Small marker chromosome and monosomy 7 in a pediatric patient with MDS

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CELL COUNT; BONE MARROW TRANSPLANTATION; CASE REPORT; CLINICAL FEATURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; IMMUNOPHENOTYPING; LETTER; MARKER CHROMOSOME; MONOSOMY 7; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; SCHOOL CHILD; SIGNAL DETECTION; SYMPTOM;

EID: 38149065985     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2007.10.015     Document Type: Letter
Times cited : (1)

References (10)
  • 1
    • 0037325661 scopus 로고    scopus 로고
    • A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases
    • Hasle H., Niemeyer C.M., Chessells J., Baumann I., Bennett J.M., Kerndrup G., and Head D.R. A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases. Leukemia 17 (2003) 277-282
    • (2003) Leukemia , vol.17 , pp. 277-282
    • Hasle, H.1    Niemeyer, C.M.2    Chessells, J.3    Baumann, I.4    Bennett, J.M.5    Kerndrup, G.6    Head, D.R.7
  • 2
    • 0036061842 scopus 로고    scopus 로고
    • A practical, comprehensive classification for pediatric myelodysplastic syndromes: the CCC system
    • [Corrected and republished from: J Pediatr Hematol Oncol 2002;24:343-352]
    • Mandel K., Dror Y., Poon A., and Freedman M.H. A practical, comprehensive classification for pediatric myelodysplastic syndromes: the CCC system. [Corrected and republished from: J Pediatr Hematol Oncol 2002;24:343-352]. J Pediatr Hematol Oncol 24 (2002) 596-605
    • (2002) J Pediatr Hematol Oncol , vol.24 , pp. 596-605
    • Mandel, K.1    Dror, Y.2    Poon, A.3    Freedman, M.H.4
  • 4
    • 33750416918 scopus 로고    scopus 로고
    • Myelodysplastic syndrome associated with monosomy 7 in childhood: a retrospective study
    • Aktas D., and Tuncbilek E. Myelodysplastic syndrome associated with monosomy 7 in childhood: a retrospective study. Cancer Genet Cytogenet 171 (2006) 72-75
    • (2006) Cancer Genet Cytogenet , vol.171 , pp. 72-75
    • Aktas, D.1    Tuncbilek, E.2
  • 7
    • 0029101518 scopus 로고
    • Fluorescence in situ hybridization analysis of minute marker chromosomes in leukemia with monosomy 7
    • Viguié F., Prigent Y., Ramond S., Baumelou E., Cadiou M., Dreyfus F., and Zittoun R. Fluorescence in situ hybridization analysis of minute marker chromosomes in leukemia with monosomy 7. Leukemia 9 (1995) 1154-1158
    • (1995) Leukemia , vol.9 , pp. 1154-1158
    • Viguié, F.1    Prigent, Y.2    Ramond, S.3    Baumelou, E.4    Cadiou, M.5    Dreyfus, F.6    Zittoun, R.7
  • 10
    • 0032739845 scopus 로고    scopus 로고
    • Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia
    • Sokolic R.A., Ferguson W., and Mark H.F. Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia. Cancer Genet Cytogenet 115 (1999) 106-113
    • (1999) Cancer Genet Cytogenet , vol.115 , pp. 106-113
    • Sokolic, R.A.1    Ferguson, W.2    Mark, H.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.