关于Xq13断点：一名急性髓性白血病患者的临床和细胞遗传学观察
On the Xq13 breakpoint: clinical and cytogenetic observations in a patient with acute myelogenous leukemia.
作者信息
Sessarego M, Bianchi Scarrà G, Giuntini P, Ajmar F
出版信息
Acta Haematol. 1983;70(2):134-6. doi: 10.1159/000206707.
PMID:6408876
Abstract
Cytogenetic study in a case of acute myelogenous leukemia revealed the presence of two identical dicentric marker chromosomes derived from an X with Xq13 breakpoints. Clinical and cytochemical findings suggest that the patient was affected by idiopathic acquired sideroblastic anemia before the acute leukemia.
摘要
对一例急性髓细胞白血病患者进行的细胞遗传学研究显示，存在两条源自X染色体且具有Xq13断点的相同双着丝粒标记染色体。临床和细胞化学检查结果表明，该患者在患急性白血病之前患有特发性获得性铁粒幼细胞贫血。
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