-transparent.png){kind=logo}
The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis. 1990
Wessex Regional Genetics Laboratory, General Hospital, Salisbury.
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.
Related Publications
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
December 1991,
The EMBO journal,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
January 1986,
Nature,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
December 1986,
Journal of medical genetics,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
May 2004,
Clinical genetics,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
June 1986,
Clinical genetics,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
April 1985,
Rinsho shinkeigaku = Clinical neurology,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
January 1988,
No to hattatsu = Brain and development,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
January 1988,
Archives of neurology,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
August 1992,
American journal of medical genetics,
D O Robinson, and
Y Boyd, and
D Cockburn, and
M N Collinson, and
I Craig, and
P A Jacobs
February 2022,
JPGN reports,
