Katrin Õunap
- Expanded newborn screening by using tandem mass-spectrometry in Estonia: a review of 18-month’ experience
- Genetic causes of hearing loss among Estonian children and their genotypephenotype correlation
- Congenital long QT syndrome
- Congenital disorders of glycosylation: an overview of the literature and a case report
- Nationwide expanded newborn screening by tandem mass spectrometry to detect treatable inborn errors of metabolism
- Genetics and genetic testing through the eyes of a medical geneticist
- Familial adenomatous polyposis: an overview and a family case report