Authors: Ryynanen, M Heinonen, S Makkonen, M Kajanoja, E Mannermaa, A Pertti, K

Citation: M. Ryynanen et al., Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies, EUR J HUM G, 7(2), 1999, pp. 212-216

Authors: Seppo, H Markku, R Marko, N Pertti, K

Citation: H. Seppo et al., Detection of trisomy 18 by double screening in a low-risk pregnant population, FETAL DIAGN, 14(1), 1999, pp. 15-19