Delon B, Lallaoui H, Abel-Lablanche C, Geneix A, Bellec V, Benkhalifa M
Cytogénétique et FIV, LMM. Mérieux Foundation, Lyon, France.
Mol Hum Reprod. 1997 May;3(5):439-43. doi: 10.1093/molehr/3.5.439.
We describe a phenotypically normal female with secondary amenorrhoea due to a translocation of genetic material involving the long arm of chromosome X (Xq28) and the long arm of chromosome Y (Yq11). We used fluorescent in situ hybridization to localize the breakpoint on the Xq. The Y chromosome breakpoint was identified using polymerase chain reaction (PCR) detection of sequence-tagged sites (STS) specific for interval 5 at Yq11.21. The relationship between this X:Y translocation and premature ovarian failure is discussed.
我们描述了一名表型正常的女性,她因涉及X染色体长臂(Xq28)和Y染色体长臂(Yq11)的遗传物质易位而出现继发性闭经。我们使用荧光原位杂交技术将Xq上的断点定位。通过聚合酶链反应(PCR)检测Yq11.21区间5特有的序列标签位点(STS)来鉴定Y染色体断点。本文讨论了这种X:Y易位与卵巢早衰之间的关系。