Myelodysplastic syndrome in a child with constitutional trisomy 8 mosaicism and normal phenotype
- 1 January 1995
- journal article
- case report
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 79 (1) , 79-81
- https://doi.org/10.1016/0165-4608(94)00099-w
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Myelodysplastic Syndromes in Childhood—Classification, Epidemiology, and TreatmentLeukemia & Lymphoma, 1994
- Atypical chronic myelogenous leukemia in a patient with trisomy 8 mosaicism syndromeAnnals of Hematology, 1993
- Acute leukemia with t(1;3)(p36;q21), evolution to t(1;3)(p36;q21),t(14;17)(q32;q21), and loss of red cell A and Leb antigensCancer Genetics and Cytogenetics, 1992
- Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in rhus, DenmarkHuman Genetics, 1991
- Quantitative variations in A, B, Ht1 and Ht2 antigens on erythrocytes in leukemia and lymphomaLeukemia Research, 1990
- Tetrasomy of chromosome 8: An interesting and rare cytogenetic phenomenon in acute nonlymphocytic leukemiaCancer Genetics and Cytogenetics, 1987
- Specific minor chromosome deletions consistently occurring in myelodysplastic syndromesCancer Genetics and Cytogenetics, 1986
- Juvenile chronic granulocytic leukemia in a patient with trisomy 8, neurofibromatosis, and prolonged Epstein-Barr virus infectionThe Journal of Pediatrics, 1983
- Acute leukemia associated with trisomy 8 mosaicism and a familial translocation 46,XY,t(7;20)(p13;p12)American Journal of Medical Genetics, 1978
- Aplastic anemia followed by leukemia in congenital trisomy 8 mosaicism:Ultrastructural studies of polymorphonuclear cells in peripheral bloodClinical Genetics, 1976