Palmer C G, Heerema N, Bull M
Department of Medical Genetics, Indiana University, Indianapolis.
Am J Med Genet. 1990 Jun;36(2):214-8. doi: 10.1002/ajmg.1320360215.
We report on 2 patients with de novo deletions of 2q and chromosome constitutions of 46,XY,del(2)(q32.3q33.3) and 46,XX,del(2) (q21q23.2), respectively. Comparisons of breakpoints of interstitial deletions show frequent correspondence to common fragile sites.
我们报告了2例分别具有2号染色体q臂从头缺失且染色体核型为46,XY,del(2)(q32.3q33.3) 和46,XX,del(2)(q21q23.2) 的患者。间质性缺失断点的比较显示,其经常与常见脆性位点相对应。