Duplication 1q as primary and 3q in t(3;13) as secondary aberration in Fanconi anemia: Implications and literature review
Author:
Publisher
Walter de Gruyter GmbH
Subject
Oncology,Hematology
Reference16 articles.
1. Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean?;Alter;Br J Haematol,1993
2. Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor;Tönnies;Blood,2003
3. Diagnosis of myelodysplastic syndrome among a cohort of 119 patients with Fanconi anemia: morphologic and cytogenetic characteristics;Cioc;Am J Clin Pathol,2010
4. Numerical chromosomal changes and risk of development of myelodysplastic syndrome-acute myeloid leukemia in patients with Fanconi anemia;Mehta;Cancer Genet Cytogenet,2010
5. Spontaneous abrogation of the G2 DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients;Ceccaldi;J Clin Invest,2011
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1. Rare cytogenetic abnormalities in MDS evolving from fanconi anemia-A case report;IP Journal of Diagnostic Pathology and Oncology;2023-01-15
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