一种结肠癌细胞系中的单染色体缺陷，1q部分三体性。
Single chromosome defect, partial trisomy 1q, in a colon cancer cell line.
作者信息
Jenkyn D J, Whitehead R H, House A K, Maley M A
出版信息
Cancer Genet Cytogenet. 1987 Aug;27(2):357-60. doi: 10.1016/0165-4608(87)90019-7.
PMID:3594419
Abstract
The characterization of a single chromosome defect previously reported in a case of inherited nonpolyposis colorectal cancer is the essence of this communication. The defect, originally described as 13p+, is now being defined and the karyotype designated as 46,XY,-13,+der(13)t(1;13)(q32.1;p11).
摘要
先前在一例遗传性非息肉病性结直肠癌病例中报道的单个染色体缺陷的特征是本交流的核心内容。该缺陷最初被描述为13p+，现在正在进行明确界定，其核型被指定为46,XY,-13,+der(13)t(1;13)(q32.1;p11)。
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