Hecht T, Cooke H J, Cerrillo M, Meer B, Reck G, Hameister H
Hum Genet. 1980;54(3):303-7. doi: 10.1007/BF00291573.
An unbalanced Y to X translocation due to a de novo mutation is described in a female with some clinical features of the Turner syndrome. Her karyotype is defined as 46,X,t(X;Y)(Xp11.2;Yq11). Hae III restriction analysis revealed an amount of male-specific DNA sequences in the normal male range. DNA replication analysis showed that in all cells studied the translocation X chromosome was late replicating and that the X segment of the translocation chromosome was later replicating while replication of the Y segment varied. A serologic test indicated a reduced titer of H-Y antigen, and biochemical studies for the enzyme steroid sulfatase revealed activity in the male range.
在一名具有特纳综合征某些临床特征的女性中,描述了由于新发突变导致的不平衡Y向X易位。她的核型定义为46,X,t(X;Y)(Xp11.2;Yq11)。Hae III限制性分析显示男性特异性DNA序列的量在正常男性范围内。DNA复制分析表明,在所研究的所有细胞中,易位的X染色体复制较晚,易位染色体的X片段复制更晚,而Y片段的复制情况各异。血清学检测表明H-Y抗原滴度降低,对类固醇硫酸酯酶的生化研究显示其活性在男性范围内。