Results for Genetics
Impact Case Study | June 18, 2018
The fourth culprit for Larsen Syndrome
Saudi scientists identify a new gene implicated in the complex musculo-skeletal and eye condition known as Larsen syndrome.
Impact Case Study | September 12, 2018
Uncovering autism genetics in Arabs
Saudi Human Genome Project discovers mutations linked to autism in Saudi families.
Impact Case Study | September 20, 2018
Uncovering the elusive causes of fetal death
Molecular autopsy reveals gene variants not previously associated with pregnancy loss and diseases.
Impact Case Study | February 26, 2019
Unlocking the origin of a severe neurological disorder
Gene sequencing brings the origin of a fatal neurological genetic disease to light.
Impact Case Study | April 17, 2019
Genetic study uncovers Ehlers-Danlos syndrome mutation
Scientists find links between a rare connective tissue disorder and mutations in a wound-healing gene called AEBP1.