Drop by drop
Katelyn Denbow lives with Alström syndrome, a rare genetic disease. Day after day, a team at The Jackson Laboratory works toward a cure.
Katelyn Denbow lives with Alström syndrome, a rare genetic disease. Day after day, a team at The Jackson Laboratory works toward a cure.
Rich Gurin knows how to catch people's attention, whether he's talking about crayons or better health.
The Laboratory enters the genomic research era with a new DNA sequencer that opens a world of opportunities.
Duchenne muscular dystrophy has no cure. Yet. An amazing family is working with the Laboratory to change that.
John Fitzpatrick makes sure the Laboratory's facilities function well and as efficiently as possible.