Wajntal A, Gonzalez C H, Koiffmann C P, de Souza D H
Am J Med Genet. 1985 Feb;20(2):265-9. doi: 10.1002/ajmg.1320200209.
We report on a family in which a maternal translocation (7;9) (7qter----7p22::9p13----9pter; 9qter----9p13) resulted in 2 sibs with dup(9p) syndrome, one sib with the same balanced constitution as the mother, and one normal boy.
我们报告了一个家族,其中母亲的染色体易位(7;9)(7qter----7p22::9p13----9pter;9qter----9p13)导致2名同胞患有9号染色体短臂重复综合征,一名同胞具有与母亲相同的平衡核型,还有一名正常男孩。