Biegel J A, Meek R S, Parmiter A H, Conard K, Emanuel B S
Division of Human Genetics and Molecular Biology, Children's Hospital of Philadelphia, PA 19104.
Genes Chromosomes Cancer. 1991 Nov;3(6):483-4. doi: 10.1002/gcc.2870030612.
Cytogenetic studies of a rhabdomyosarcoma of mixed embryonal and alveolar histology in an 11-month-old male revealed a single structural abnormality, t(1;13)(p36;q14). This abnormality may define a subset of patients with a variant of the t(2;13)(q35;q14) translocation frequently seen in alveolar rhabdomyosarcoma.
对一名11个月大男性的混合胚胎型和腺泡型组织学横纹肌肉瘤进行的细胞遗传学研究显示存在单一结构异常,即t(1;13)(p36;q14)。这种异常可能定义了一部分患有t(2;13)(q35;q14)易位变体的患者,该易位在腺泡状横纹肌肉瘤中经常出现。