Characterization of t(15;21) translocations in myeloid disorders
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https://www.ncbi.nlm.nih.gov/sra/SRP061835
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资源简介：
We report on two novel t(15;21) alterations [t(15;21)(q24;q22) and t(15;21)(q21;q22)], which led to concurrent disruption of RUNX1 and two translocation partner genes encoding for transcription factors (SIN3A, TCF12) Overall design: Examination of four different patients with myeloid disorders. 2 out of 4 have been analyzed by means RNAseq
创建时间：
2017-09-17
