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. 1990 Oct-Dec;56(2-3):135-40.
doi: 10.1017/s0016672300035217.

The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis

D O Robinson  1 , Y Boyd, D Cockburn, M N Collinson, I Craig, P A Jacobs
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The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis

D O Robinson et al. Genet Res. 1990 Oct-Dec.

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.

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