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Lack of TP53 and FMS gene mutations in children with myelodysplastic syndrome
(Elsevier Science Inc, New York, 2006)
Myelodysplastic syndromes (MDS) are rare disorders in children. Molecular mechanisims underlying MDS in children are not yet completely understood. Considering the role of FMS and TP53 gene mutations in adult MDS patients, ...
Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes
(Elsevier Science Inc, New York, 2004)
In children, myelodysplastic syndromes (MDS) represent less then 10% of all hematological malignancies; consequently, molecular genetic studies dealing with this group of patients are scarce. We have analyzed 35 archival ...