Málstofa: Genetics and diseases
- Málstofa: 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
- Málstofa: 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
- Málstofa: Genetics and diseases
A mechanistic hypothesis explaining the occurrence of two distinct phenotypes from the CREBBP/EP300 genes
- Salur: B
- Málstofa: Genetics and diseases
The predictive value of a polygenic risk score for heart failure in the AGES cohort
- Salur: B
