Susan Mathew
Department of Pathology and Laboratory Medicine
St. Jude Children's Research Hospital
Memphis
TN 38105-2794
USA
Name/email consistency: high
- A complex variant t(8;21) involving chromosome 3 in a child with acute myeloblastic leukemia with eosinophilia (AML M4Eo). Mathew, S., Shurtleff, S., Ribeiro, R.C., Behm, F.G., Raimondi, S.C. Leuk. Lymphoma (2003)
- Complex t(X;18)(p11.2;q11.2) with a pericentric inversion of the X chromosome in an adolescent boy with synovial sarcoma. Mathew, S., Dalton, J., Riedley, S., Spunt, S.L., Hill, D.A. Cancer Genet. Cytogenet. (2002)
- Novel cryptic, complex rearrangements involving ETV6-CBFA2 (TEL-AML1) genes identified by fluorescence in situ hybridization in pediatric patients with acute lymphoblastic leukemia. Mathew, S., Shurtleff, S.A., Raimondi, S.C. Genes. Chromosomes. Cancer (2001)
- Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodysplastic syndrome following treatment for a primitive neuroectodermal tumor. Mathew, S., Head, D., Rodriguez-Galindo, C., Raimondi, S.C. Leuk. Lymphoma (2000)
- Concurrent translocations of MLL and CBFA2 (AML1) genes with new partner breakpoints in a child with secondary myelodysplastic syndrome after treatment of acute lymphoblastic leukemia. Mathew, S., Head, D., Rubnitz, J.E., Raimondi, S.C. Genes. Chromosomes. Cancer (2000)
