Nielsen L B, Boczkowski K, Mikkelsen M, Dahl G, Andersen E
Hum Genet. 1982;61(1):12-7. doi: 10.1007/BF00291323.
Four girls with some clinical symptoms of Turner's syndrome had Xq duplication and Xp deficiency, their karyotypes being 46,X,dup(X)(p113;q11), 46,X,dup(X)(p212;q211), 46,X,dup(X)(p225;q13), and 46,X,dup(X)(p222;q213). No mosaicism was found. The major clinical findings, short stature, lack of pterygium colli, and no continuous gamete production, are compared with those in three previously published cases.
四名有特纳综合征某些临床症状的女孩存在Xq重复和Xp缺失,其核型分别为46,X,dup(X)(p113;q11)、46,X,dup(X)(p212;q211)、46,X,dup(X)(p225;q13)和46,X,dup(X)(p222;q213)。未发现嵌合体现象。将主要临床发现,如身材矮小、无颈蹼以及无持续配子生成,与之前发表的三例病例进行了比较。