6 results
- Digital Images
- Online
Duchenne muscular dystrophy carrier female
Wessex Reg. Genetics Centre- Digital Images
- Online
Genetics frame of reference - the size of various genetic components, including DNA, a base pair, various sizes of deletions, chromosomes and genes are listed and compared with more familiar objects such as the Solar System, planets, cities, hospitals, wards, and so on.
Wessex Reg. Genetics Centre- Digital Images
- Online
Duchenne muscular dystrophy - normal female, chromosomes have been highlighted by a fluorescent probe for exon 45/47 (note the double yellow band). This disorder is caused by a recessive gene on the X chromosome, so is normally shown only by males, who lack a second X chromosome. The condition starts with difficulty in walking and climbing stairs in early childhood, usually resulting in confinement to a wheelchair by the age of 10, with death from respiratory infection or cardiac failure by about the age of 20.
Wessex Reg. Genetics Centre- Videos
Muscle disorders in children.
Date: 1976- Archives and manuscripts
Correspondence with Jan van den Bosch
Date: Oct 1962 - Dec 1962Reference: PENROSE/2/45/1/12Part of: L. S. Penrose Papers- Videos
Last hope clinic.
Date: 2007