Schwaab R, Oldenburg J, Higuchi M, Ludwig M, Kochhan L, Horst J, Brackmann H H, Egli H, Olek K
Institut für Experimentelle Hämatologie und Bluttransfusionswesen, Universität Bonn, Federal Republic of Germany.
Blut. 1988 Aug;57(2):85-90. doi: 10.1007/BF00319731.
From 46 families of predominantly German origin, afflicted with haemophilia A, 178 females were tested for carrier status. Two polymorphic restriction endonuclease sites, the extragenic marker locus DXS 52 (St 14 probe) and the intragenic Bcl I RFLP were investigated in these families. In some cases the results were corroborated by identifying (i) deletions within the factor VIII:C gene and (ii) eliminating a restriction endonuclease site. Two new alleles of the DXS 52 marker locus were found. According to this strategy, 27 women were classified as carriers and 74 as non-carriers. Forty-six women were classified as carriers according to pedigree analysis. Twenty-five females of families with sporadic cases and 6 test persons, who had mothers who where homozygous for the marker alleles, were diagnosed by additional use of conventional carrier detection.
在46个主要为德国血统且患有甲型血友病的家族中,对178名女性进行了携带者状态检测。在这些家族中研究了两个多态性限制性内切酶位点,即基因外标记位点DXS 52(St 14探针)和基因内Bcl I限制性片段长度多态性。在某些情况下,通过鉴定(i)凝血因子VIII:C基因内的缺失和(ii)消除一个限制性内切酶位点来证实结果。发现了DXS 52标记位点的两个新等位基因。根据这一策略将27名女性分类为携带者,74名女性分类为非携带者。根据系谱分析,46名女性被分类为携带者。通过额外使用传统携带者检测方法,对25名散发病例家族的女性和6名其母亲为标记等位基因纯合子的受测者进行了诊断。