A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemia

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A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemia

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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A unique cytogenetic abnormali ...... itive chronic myeloid leukemia

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A unique cytogenetic abnormali ...... itive chronic myeloid leukemia

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A unique cytogenetic abnormali ...... itive chronic myeloid leukemia

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A unique cytogenetic abnormali ...... itive chronic myeloid leukemia

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A unique cytogenetic abnormali ...... itive chronic myeloid leukemia

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A unique cytogenetic abnormali ...... itive chronic myeloid leukemia

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P1476

A unique cytogenetic abnormali ...... itive chronic myeloid leukemia

@en

P2093

Abdulsamad Wafa

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Faten Moassass

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Thomas Liehr

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Walid Al-Achkar

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P2860

cDNA array-CGH profiling identifies genomic alterations specific to stage and MYCN-amplification in neuroblastoma

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Specificities of protein-protein and protein-DNA interaction of GABP alpha and two newly defined ets-related proteins

Cell surface tumor endothelial markers are conserved in mice and humans

Microdissection based high resolution multicolor banding for all 24 human chromosomes.

The BCL11 gene family: involvement of BCL11A in lymphoid malignancies.

A novel t(6;14)(q25-q27;q32) in acute myelocytic leukemia involves the BCL11B gene.

Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.

Chromosomal translocations in cancer.

Hybrid acute leukaemia.

P304

209-212

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scholarly article

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10.3892/OL.2012.720

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2012-05-17T00:00:00Z

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230586683

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22844355

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P921

chronic myeloid leukemia

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3402735

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