Lykilorð: Genetic disease
- Seminar: Genetics and diseases
FAM118A a candidate gene for a new syndrome of mild developmental delay, distal arthrogryposis, exostosis of manubrium sterni, missing adult teeth, and amblyopia
- Salur: B
- Seminar: Genetics and diseases
Prevalence of myotonic dystrophy type 1 in Iceland is three times the world average with 77% of cases identified through indirect family-mediated cascade testing
- Salur: B
