Jani Sait S N, Raimondi S C, Look A T, Gill H, Thirman M, Diaz M O, Shows T B
Department of Human Genetics, Roswell Park Cancer Institute, Buffalo, New York 14263.
Genes Chromosomes Cancer. 1993 May;7(1):28-31. doi: 10.1002/gcc.2870070105.
Translocations involving 11q23 have been shown to be a consistent finding in human hematopoietic malignancies and in some constitutional abnormalities. The identification of a gene, MLL (myeloid/lymphoid or mixed-lineage leukemia), that spans the breakpoints in four different recurrent 11q23 translocations was recently reported. We describe a rare (11;12)(q23;p13) translocation, observed in leukemic cells from a patient with acute lymphoblastic leukemia, which also disrupts this gene.
涉及11q23的易位已被证明在人类造血系统恶性肿瘤和一些先天性异常中是一个一致的发现。最近报道了一个跨越四种不同的常见11q23易位断点的基因,即MLL(髓系/淋巴系或混合谱系白血病)基因。我们描述了一种罕见的(11;12)(q23;p13)易位,在一名急性淋巴细胞白血病患者的白血病细胞中观察到,该易位也破坏了这个基因。