Turleau C, de Grouchy J, Chavin-Colin F, Junien C, Séger J, Schlienger P, Leblanc A, Haye C
Cancer Genet Cytogenet. 1985 Apr 15;16(4):321-34. doi: 10.1016/0165-4608(85)90240-7.
Sixty-six retinoblastoma patients were investigated using high resolution banding techniques, sister chromatid exchange (SCE) studies, and esterase-D phenotype determination and dosage. Seven patients (in six families) were found to be carriers of a rearrangement of band 13q14 due to de novo deletions, apparently balanced de novo translocations, or parental insertions. The possible role of submicroscopic parental insertions is suggested to explain transmission of nonchromosomal forms through unaffected carriers.
采用高分辨率显带技术、姐妹染色单体交换(SCE)研究以及酯酶-D表型测定和剂量分析,对66例视网膜母细胞瘤患者进行了调查。发现7例患者(来自6个家族)是13q14带重排的携带者,重排原因包括新生缺失、明显平衡的新生易位或亲代插入。有人提出亚显微亲代插入的可能作用,以解释非染色体形式通过未受影响的携带者进行传递的现象。