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New recurrent deletions in the PPAR gamma and TP53 genes are associated with childhood myelodysplastic syndrome
(Pergamon-Elsevier B.V. Ltd, 2009-01-01)
Myelodysplastic syndrome (MDS) is a rare hematological malignancy in children. It was performed FISH analysis in 19 pediatric MDS patients to investigate deletions involving the PPAR gamma and TP53 genes. Significant losses ...
New recurrent deletions in the PPAR gamma and TP53 genes are associated with childhood myelodysplastic syndrome
(Pergamon-Elsevier B.V. Ltd, 2009-01-01)
Myelodysplastic syndrome (MDS) is a rare hematological malignancy in children. It was performed FISH analysis in 19 pediatric MDS patients to investigate deletions involving the PPAR gamma and TP53 genes. Significant losses ...
B lineage acute lymphoblastic leukemia transformation in a child with juvenile myelomonocytic leukemia, type 1 neurofibromatosis and monosomy of chromosome 7 - Possible implications in the leukemogenesis
(Elsevier B.V., 2003-04-01)
This report describes the case of an 8-month-old infant with a diagnosis of juvenile myelomonocytic leukemia (JMML) and type I neurofibromatosis that presented progression to B lineage acute lymphoid leukemia (ALL). The ...
B lineage acute lymphoblastic leukemia transformation in a child with juvenile myelomonocytic leukemia, type 1 neurofibromatosis and monosomy of chromosome 7 - Possible implications in the leukemogenesis
(Elsevier B.V., 2003-04-01)
This report describes the case of an 8-month-old infant with a diagnosis of juvenile myelomonocytic leukemia (JMML) and type I neurofibromatosis that presented progression to B lineage acute lymphoid leukemia (ALL). The ...
New recurrent deletions in the PPAR gamma and TP53 genes are associated with childhood myelodysplastic syndrome
(PERGAMON-ELSEVIER SCIENCE LTD, 2009)
Myelodysplastic syndrome (MDS) is a rare hematological malignancy in children. It was performed FISH analysis in 19 pediatric MDS patients to investigate deletions involving the PPAR gamma and TP53 genes. Significant losses ...
New recurrent deletions in the PPAR gamma and TP53 genes are associated with childhood myelodysplastic syndrome
(Pergamon-Elsevier B.V. Ltd, 2014)
Investigação citogenética na síndrome mielodisplásica infantil
(Universidade Estadual Paulista (Unesp), 2006-10-25)
A Síndrome Mielodisplásica (SMD) consiste em um grupo heterogêneo de doenças hematológicas de origem monoclonal e potencialmente maligna. É caracterizada por uma hematopoese ineficaz das células-tronco pluripotentes e ...
Investigação citogenética na síndrome mielodisplásica infantil
(Universidade Estadual Paulista (Unesp), 2006-10-25)
A Síndrome Mielodisplásica (SMD) consiste em um grupo heterogêneo de doenças hematológicas de origem monoclonal e potencialmente maligna. É caracterizada por uma hematopoese ineficaz das células-tronco pluripotentes e ...
Investigação citogenética na síndrome mielodisplásica infantil
(Universidade Estadual Paulista (UNESP), 2014)