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Cytogenetics Database CytoD 1.0

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Query: inv(11)(p15q22)

Search Results:

inv(11)(p15q22)     11p15 translocations involving the NUP98 gene in childhood therapy-related acute myeloid leukemia/myelodysplastic syndrome. Genes Chromosomes Cancer. 1999 Nov;26(3):215-20.
inv(11)(p15q22)     Inversion of chromosome 11 inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: identification of a P1 clone spanning the 11q22 breakpoint. Genes Chromosomes Cancer. 1997 Jul;19(3):150-5.
inv(11)(p15q22)     The inv(11)(p15q22) chromosome translocation of therapy-related myelodysplasia with NUP98-DDX10 and DDX10-NUP98 fusion transcripts. Int J Hematol. 1999 Apr;69(3):160-4.
inv(11)(p15q22)     The t(11;20)(p15;q11) chromosomal translocation associated with therapy-related myelodysplastic syndrome results in an NUP98-TOP1 fusion. Blood. 1999 Nov 1;94(9):3258-61.
inv(11)(p15q22)     The inv(11)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase gene, DDX10. Blood. 1997 Jun 1;89(11):3936-44.

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