Authors: Mantyjarvi, M Nurmenniemi, P Partanen, J Myohanen, T Peippo, M Alitalo, T

Citation: M. Mantyjarvi et al., Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy, ACT OPHTH S, 79(4), 2001, pp. 359-365

Authors: Huopaniemi, L Tyynismaa, H Rantala, A Rosenberg, T Alitalo, T

Citation: L. Huopaniemi et al., Characterization of two unusual RS1 gene deletions segregating in Danish retinoschisis families, HUM MUTAT, 16(4), 2000, pp. 307-314

Authors: Huopaniemi, L Rantala, A Forsius, H Somer, M de la Chapelle, A Alitalo, T

Citation: L. Huopaniemi et al., Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland, EUR J HUM G, 7(3), 1999, pp. 368-376

Authors: Huopaniemi, L Fellman, J Rantala, A Eriksson, A Forsius, H De la Chapelle, A Alitalo, T

Citation: L. Huopaniemi et al., Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 gene, ANN HUM GEN, 63, 1999, pp. 521-533

Authors: Shiraishi, M Oates, AJ Li, X Hosoda, F Ohki, M Alitalo, T Lerman, LS Sekiya, T

Citation: M. Shiraishi et al., The isolation of CpG islands from human chromosomal regions 11q13 and Xp22by segregation of partly melted molecules, NUCL ACID R, 26(24), 1998, pp. 5544-5550