Schwartz C, Fitch N, Phelan M C, Richer C L, Stevenson R
Hum Genet. 1987 May;76(1):54-7. doi: 10.1007/BF00283050.
Two sisters with premature menopause and a small deletion of the long arm of one of their X chromosomes [del (X)(pter----q26.3:)] were investigated with polymorphic DNA probes near the breakpoint. The deleted chromosome retained the factor IX (F9) locus and the loci DXS51 (52A) and DXS100 (pX45h), which are proximal to F9. However, the factor VIII (F8) locus was not present, nor were two loci tightly linked to this locus, DXS52 (St14) and DXS15 (DX13). This deletion refines the location of the F9 locus to Xq26 or to the interface Xq26/Xq27, thus placing it more proximally than has been previously reported. The DNA obtained from these patients should be valuable in the mapping of future probes derived from this region of the X chromosome.
对两名患有过早绝经且其一条X染色体长臂存在小片段缺失[del(X)(pter----q26.3:)]的姐妹,使用靠近断点处的多态性DNA探针进行了研究。缺失的染色体保留了因子IX(F9)基因座以及位于F9近端的基因座DXS51(52A)和DXS100(pX45h)。然而,因子VIII(F8)基因座不存在,与该基因座紧密连锁的两个基因座DXS52(St14)和DXS15(DX13)也不存在。这种缺失将F9基因座的位置精确到Xq26或Xq26/Xq27界面,因此其位置比先前报道的更靠近近端。从这些患者获得的DNA对于绘制未来源自X染色体该区域的探针图谱将具有重要价值。