논문KCI 등재
Isochromosome 1q in Childhood Burkitt Lymphoma: The First Reported Case in Korea
대한진단검사의학회 (Korean Society For Laboratory Medicine)|2015.11|Annals of Laboratory Medicine|제35권 제6호|pp. 663-665
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참고문헌 (10)
- Djordjević V, "Pattern of trisomy 1q in hematological malignancies: a single institution experience", Cancer Genet Cytogenet, 186, pp.12~18 (2008)
- Hawkins JM, "Isochromosome 1q in acute monocytic leukemia: a new nonrandom association", Genes Chromosomes Cancer, 5, pp.181~183 (1992)
- Lai JL, "Cytogenetic studies in 30 patients with Burkitt’s lymphoma or L3 acute lymphoblastic leukemia with special reference to additional chromosome abnormalities", Ann Genet, 32, pp.26~32 (1989)
- Roug AS, "Supernumerary isochromosome 1, idic(1)(p12), leading to tetrasomy 1q in Burkitt lymphoma", Cytogenet Genome Res, 142, pp.7~13 (2014)
- Maria Murga Penas E, "Comprehensive cytogenetic and molecular cytogenetic analysis of 44 Burkitt lymphoma cell lines: secondary chromosomal changes characterization, karyotypic evolution, and comparison with primary samples", Genes Chromosomes Cancer, 53, pp.497~515 (2014)
- Wodzinski MA, "Chromosomes in childhood acute lymphoblastic leukaemia: karyotypic patterns in disease subtypes", J Clin Pathol, 44, pp.48~51 (1991)
- Navid F, "Acute lymphoblastic leukemia with the(8;14)(q24;q32)translocation and FAB L3 morphology associated with a B-precursor immunophenotype : the Pediatric Oncology Group experience", Leukemia, 13, pp.135~141 (1999)
- Havelange V, "Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement", Genes Chromosomes Cancer, 52, pp.81~92 (2013)
- de Souza MT, "Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia", lymphoma cases with 8q24 rearrangement at diagnosis, 2011, pp.93, 232~236
- de la Chapelle A., "How do human isochromosomes arise?", Cancer Genet Cytogenet, 5, pp.173~179 (1982)
관련 논문AI추천
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