Stephens K, Riccardi V M, Rising M, Ng S, Green P, Collins F S, Rediker K S, Powers J A, Parker C, Donis-Keller H
Department of Human Genetics, Collaborative Research, Inc., Bedford, Massachusetts 01730.
Genomics. 1987 Dec;1(4):353-7. doi: 10.1016/0888-7543(87)90037-1.
A locus for von Recklinghausen neurofibromatosis (NF1) has recently been mapped near the chromosome 17 centromere. We have extended these linkage studies by genotyping 45 NF1 families with three DNA probes known to be linked to the chromosome 17 centromeric region. Of 34 families informative for NF1 and at least one of the three probes, 28 families show no recombinants with the disease gene. These data provide additional support for genetic homogeneity of NF1 and for a primary NF1 locus linked to the chromosome 17 centromere. Among the informative families were 7 families with apparent new NF1 mutations. Our data suggest that these mutations are probably at the chromosome 17 NF1 locus.
冯·雷克林霍增氏神经纤维瘤病(NF1)的一个基因座最近已被定位到17号染色体着丝粒附近。我们通过使用已知与17号染色体着丝粒区域连锁的三种DNA探针,对45个NF1家族进行基因分型,扩展了这些连锁研究。在对NF1和这三种探针中的至少一种具有信息性的34个家族中,有28个家族未出现与疾病基因的重组。这些数据为NF1的遗传同质性以及与17号染色体着丝粒连锁的主要NF1基因座提供了额外支持。在这些具有信息性的家族中有7个家族存在明显的新NF1突变。我们的数据表明,这些突变可能位于17号染色体的NF1基因座上。