Lohmann D R, Brandt B, Oehlschläger U, Göttmann E, Höpping W, Passarge E, Horsthemke B
Institut für Humangenetik, Universitätsklinikum Essen, Germany.
Ophthalmic Genet. 1995 Dec;16(4):135-42. doi: 10.3109/13816819509057854.
Predictive testing using molecular analysis is an integral part of contemporary retinoblastoma management. We have made extensive use of segregation analysis for risk assessment in both familial and sporadic disease. Investigation of loss of heterozygosity in tumor samples proved to be invaluable for the identification of linkage phase. In many families, however, accurate carrier risk assessment depends on direct identification of the causative R B I mutation. Consequently, we have developed methods for rapid mutation screening. Using these techniques, mutation analysis can now be offered to an increasing number of individuals.
使用分子分析进行预测性检测是当代视网膜母细胞瘤治疗的一个组成部分。我们在家族性和散发性疾病的风险评估中广泛使用了分离分析。事实证明,对肿瘤样本进行杂合性缺失研究对于确定连锁相非常重要。然而,在许多家族中,准确的携带者风险评估取决于直接鉴定致病的RB1突变。因此,我们开发了快速突变筛查方法。利用这些技术,现在可以为越来越多的个体提供突变分析。