Helena Kääriäinen

hkaaria@utu.fi

Publications

Translation of a research-based genetic test on rare syndrome into clinical service testing with Sotos syndrome as an example (2012)
- Genetic Testing and Molecular Biomarkers
Pohjola P, Peippo M, Penttinen MT, Elenius K, Kääriäinen H
(A1 Refereed original research article in a scientific journal)
Terminal 3p deletions in two families-correlation between molecular karyotype and phenotype (2010)
- American Journal of Medical Genetics Part A
Pohjola P, de Leeuw N, Penttinen M, Kääriäinen H
(A1 Refereed original research article in a scientific journal)