Publications

Export 2 results:
Author Title [ Year(Asc)]
Filters: Author is Õiglane-Shlik, Eve  [Clear All Filters]
2020
Õunap, K. et al. PEHO syndrome caused by compound heterozygote variants in ZNHIT3 gene. Eur J Med Genet 63, 103660 (2020).
2019
Yakoreva, M. et al. A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016. Eur J Hum Genet 27, 1649-1658 (2019).