Pagano L, Fioretti G, Vetrella M, Risolo E, Casullo C, Celona A, Renda S, Rinaldi A, Ventruto V
Ann Genet. 1980;23(3):173-5.
The authors report on a family with a t(3;6). All four members of a sibship were carriers of the balanced translocation and two have had children with multiple malformations. The proband, six months old, had the karyotype 46,XY, t(3;6) (p26;p21) der pat. His clinical features were typical of the trisomy 6p syndrome. HLA typing data failed demonstrate both paternal haplotypes in the propositus.
作者报告了一个患有t(3;6)的家族。一个同胞家族的所有四名成员都是平衡易位的携带者,其中两人育有患有多种畸形的子女。先证者为6个月大的男性,其核型为46,XY, t(3;6) (p26;p21) der pat。他的临床特征是典型的6p三体综合征。HLA分型数据未能在该先证者中显示出父本的两个单倍型。