Duchenne muscular dystrophy deletion, FISH
- Wessex Reg. Genetics Centre
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Description
Human chromosomes highlighted by fluorescent
probes which bind to specific sequences of DNA.
The FISH (fluorescence in situ hybridisation)
study is of a female heterozygous for a deletion
in the Duchenne muscular dystrophy (DMD) gene. The
DMD cosmid probe is red, the X chromosome
centromeres are green.
See B0000325C for control.
Image by Dr John Crolla.