Using pulsed-field gel electrophoresis and 12 Xp21-derived DNA probes, we have constructed a continuous restriction map spanning more than 4 million base pairs (4 Mbp), including the Duchenne muscular dystrophy gene of more than 2 Mbp. This detailed map is part of a less detailed map spanning 10 Mbp, also spanning the genes for glycerol kinase and congenital adrenal hypoplasia, constructed under electrophoresis conditions which separated DNA fragments in the range 200 to 4000 kbp. DNA from three different tissues was analyzed, and differential methylation was observed
The application of recombinant DNA technology to prenatal diagnosis of many recesslvely inherited X-...
In recent years, the molecular understanding of human inherited disorders has been advanced by the i...
A DNA deletion in a patient with Becker muscular dystrophy (BMD) has been delineated by restriction ...
Duchenne muscular dystrophy (DMD) and the less severe Becker muscular dystrophy (BMD) are human X-li...
The gene responsible for Duchenne and Becker muscular dystrophy has been assigned to band Xp21 of th...
Genomic DNA from a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adre...
Twenty-nine deletion breakpoints were mapped in 220 kb of the DXS164 locus relative to potential exo...
Several genes involved in human genetic diseases map to the Xq22 band on the long arm of the human X...
Deletion is a common cause of Duchenne muscular dystrophy (DMD). Field-inversion gel electrophoresis...
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...
We report on the physical ordering of genes in a relatively small area of chromosome 19, segment q13...
Heavy methylation of restriction sites in the relevant chromosomal region can be a major problem in ...
McLeod syndrome, characterized by acanthocytosis and the absence of a red-blood-cell Kell antigen (K...
The inheritance of Duchenne muscular dystrophy in 25 families was studied with 13 X chromosome speci...
The application of recombinant DNA technology to prenatal diagnosis of many recesslvely inherited X-...
In recent years, the molecular understanding of human inherited disorders has been advanced by the i...
A DNA deletion in a patient with Becker muscular dystrophy (BMD) has been delineated by restriction ...
Duchenne muscular dystrophy (DMD) and the less severe Becker muscular dystrophy (BMD) are human X-li...
The gene responsible for Duchenne and Becker muscular dystrophy has been assigned to band Xp21 of th...
Genomic DNA from a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adre...
Twenty-nine deletion breakpoints were mapped in 220 kb of the DXS164 locus relative to potential exo...
Several genes involved in human genetic diseases map to the Xq22 band on the long arm of the human X...
Deletion is a common cause of Duchenne muscular dystrophy (DMD). Field-inversion gel electrophoresis...
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...
We report on the physical ordering of genes in a relatively small area of chromosome 19, segment q13...
Heavy methylation of restriction sites in the relevant chromosomal region can be a major problem in ...
McLeod syndrome, characterized by acanthocytosis and the absence of a red-blood-cell Kell antigen (K...
The inheritance of Duchenne muscular dystrophy in 25 families was studied with 13 X chromosome speci...
The application of recombinant DNA technology to prenatal diagnosis of many recesslvely inherited X-...
In recent years, the molecular understanding of human inherited disorders has been advanced by the i...
A DNA deletion in a patient with Becker muscular dystrophy (BMD) has been delineated by restriction ...