The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis.
作者信息
Robinson D O, Boyd Y, Cockburn D, Collinson M N, Craig I, Jacobs P A
机构信息
Wessex Regional Genetics Laboratory, General Hospital, Salisbury.
出版信息
Genet Res. 1990 Oct-Dec;56(2-3):135-40. doi: 10.1017/s0016672300035217.
PMID:2272503
Abstract
The parental origin of 3 de novo X-autosome translocations in females with Duchenne Muscular Dystrophy (DMD) was studied by means of methylation analysis using the X-linked probe M27 beta. In all three the translocation was found to be paternal in origin. The parental origin of X-autosome translocations in females with and without DMD is compared with other structural abnormalities of the X and with autosomal translocations.
摘要
Zotero 插件