inv(12)(q15q24)：一种与骨髓增生异常相关的非随机变化？
Inv(12)(q15q24): a nonrandom change associated with myelodysplasia?
作者信息
Scantamburlo G, Lampertz S, Croisiau C, Jamar M, Koulischer L, Herens C
机构信息
Department of Human Genetics, University of Liège, Center for Human Genetics, Sart Tilman, Belgium.
出版信息
Cancer Genet Cytogenet. 2000 Sep;121(2):206-7. doi: 10.1016/s0165-4608(99)00172-7.
Abstract
A patient with refractory anemia and a paracentric inversion of chromosome 12, inv(12)(q15q24), is described. This is the second reported case with this chromosome anomaly, suggesting that this rearrangement is a rare but nonrandom change associated with myelodysplastic syndromes.
摘要
本文描述了一名患有难治性贫血且伴有12号染色体臂内倒位inv(12)(q15q24)的患者。这是第二例报道的具有这种染色体异常的病例，提示这种重排是一种与骨髓增生异常综合征相关的罕见但非随机的改变。
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