Molecular analysis of alleles segregation at RFLPs within RB-1 gene in four families with hereditary retinoblastoma.

E Kostyk, J Wieckiewicz, A Sutkowska, H Zygulska-Mach, J J Pietrzyk
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Abstract

Four families with suspected hereditary retinoblastoma in proband and one other family member were examined by genetic segregation analysis of the RB-1 gene loci with specific RFLPs of chromosome 13. Two families, TA-6 and partially CK-46, were informative using this method. In TA-6 family healthy sister (TA-6/10) of the proband was shown not to be a carrier of the mutant RB-1 gene. These results show that the segregation analysis of RB-1 gene loci with specific RFLPs, used as the DNA markers, could be helpful in the genetic diagnosis and counselling in families with hereditary retinoblastoma.

4个遗传性视网膜母细胞瘤家族RB-1基因RFLPs等位基因分离的分子分析。
对4个先证家族和1个家族成员进行了13号染色体RB-1基因位点特异性RFLPs分离分析。两个家族,TA-6和部分CK-46,使用这种方法提供了信息。在TA-6家族中,先证者健康姐妹(TA-6/10)不携带突变的RB-1基因。这些结果表明,将RB-1基因位点与特异性RFLPs分离分析作为DNA标记,有助于遗传性视网膜母细胞瘤家庭的遗传诊断和咨询。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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