Asamoah A, North K, Doran S, Wagstaff J, Ogle R, Collins F S, Korf B R
Division of Genetics, Children's Hospital, Boston, Massachusetts 02115, USA.
Am J Med Genet. 1995 Aug 14;60(4):312-6. doi: 10.1002/ajmg.1320600410.
We report a family with a paracentric inversion of the long arm of chromosome 17 [inv(17)(q11.2q25.1)] and neurofibromatosis type one (NF1). The family was ascertained because of NF1 and multiple miscarriages. Fluorescence in situ hybridization using cosmid probes from opposite ends of the NF1 gene confirmed that the inversion disrupts the gene. Using field inversion gel electrophoresis we have found that the inversion separates cDNA probes FB5D and AE25, which are normally adjacent to one another in the NF1 gene. This is the third published report of a gross chromosomal rearrangement responsible for NF1. The features in this family are typical for NF1, and are not unusually severe.
我们报告了一个患有17号染色体长臂臂间倒位[inv(17)(q11.2q25.1)]和1型神经纤维瘤病(NF1)的家族。该家族因NF1和多次流产而被确定。使用来自NF1基因两端的黏粒探针进行荧光原位杂交证实,这种倒位破坏了该基因。通过脉冲场凝胶电泳,我们发现这种倒位使cDNA探针FB5D和AE25分离,而它们在NF1基因中通常是相邻的。这是第三篇发表的关于导致NF1的染色体大片段重排的报告。这个家族的特征是NF1的典型特征,且并不异常严重。