The inheritance of Duchenne muscular dystrophy in 25 families was studied with 13 X chromosome specific cloned DNA fragments from 10 loci in and surrounding Xp21. When multiple probes were informative, the meiotic exchange points for each meiosis were located in individual families. Neither genetic nor physical evidence indicates an unusually high recombination rate across Xp21 in these 25 families
Duchenne muscular dystrophy (DMD) and the less severe Becker muscular dystrophy (BMD) are human X-li...
Two male cousins with Duchenne muscular dystrophy were found to have different maternal dystrophin g...
A young female was diagnosed as having X-linked muscular dystrophy of the Duchenne type. Chromosome ...
The inheritance of Duchenne muscular dystrophy in 25 families was studied with 13 X chromosome speci...
Twenty-nine deletion breakpoints were mapped in 220 kb of the DXS164 locus relative to potential exo...
SUMMARY We have studied the inheritance of four cloned DNA sequences which recognise restriction fra...
SUMMARY A number of DNA probes from the short arm of the X chromosome have been used to study the in...
SUMMARY Twenty known cases of X;autosome translocations with breakpoints at Xp2l associated with Duc...
The gene responsible for Duchenne and Becker muscular dystrophy has been assigned to band Xp21 of th...
Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder for which the biochemica...
Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder for which the biochemica...
The murine locus corresponding to the human Duchenne/Becker muscular dystrophy (DMD) gene has been r...
By the use of a series of closely linked DNA probes detecting restriction fragment length polymorphi...
The linkage relationships of the gene for Emery-Dreifuss muscular dystrophy have been analysed in a ...
A number of DNA probes from the short arm of the X chromosome have been used to study the inheritanc...
Duchenne muscular dystrophy (DMD) and the less severe Becker muscular dystrophy (BMD) are human X-li...
Two male cousins with Duchenne muscular dystrophy were found to have different maternal dystrophin g...
A young female was diagnosed as having X-linked muscular dystrophy of the Duchenne type. Chromosome ...
The inheritance of Duchenne muscular dystrophy in 25 families was studied with 13 X chromosome speci...
Twenty-nine deletion breakpoints were mapped in 220 kb of the DXS164 locus relative to potential exo...
SUMMARY We have studied the inheritance of four cloned DNA sequences which recognise restriction fra...
SUMMARY A number of DNA probes from the short arm of the X chromosome have been used to study the in...
SUMMARY Twenty known cases of X;autosome translocations with breakpoints at Xp2l associated with Duc...
The gene responsible for Duchenne and Becker muscular dystrophy has been assigned to band Xp21 of th...
Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder for which the biochemica...
Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder for which the biochemica...
The murine locus corresponding to the human Duchenne/Becker muscular dystrophy (DMD) gene has been r...
By the use of a series of closely linked DNA probes detecting restriction fragment length polymorphi...
The linkage relationships of the gene for Emery-Dreifuss muscular dystrophy have been analysed in a ...
A number of DNA probes from the short arm of the X chromosome have been used to study the inheritanc...
Duchenne muscular dystrophy (DMD) and the less severe Becker muscular dystrophy (BMD) are human X-li...
Two male cousins with Duchenne muscular dystrophy were found to have different maternal dystrophin g...
A young female was diagnosed as having X-linked muscular dystrophy of the Duchenne type. Chromosome ...