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Human Mutation|October 3, 2000
Characterization of two unusual RS1 gene deletions segregating in Danish retinoschisis familiesL Huopaniemi, H Tyynismaa, A Rantala, et al.Human Mutation|March 29, 2000
Identification of fifteen novel PHEX gene mutations in Finnish patients with hypophosphatemic ricketsH Tyynismaa, I Kaitila, K Näntö-Salonen, et al.Acta Neurologica Scandinavica|July 31, 2015
Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66ValP Pasanen, L Myllykangas, M Pöyhönen, et al.Journal of Medical Genetics|June 17, 2003
A new genetic locus for X linked progressive cone-rod dystrophyR Jalkanen, F Y Demirci, H Tyynismaa, et al.Pageof 1