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Authors: Nokelainen, P Heiskala, H Raininko, R Autti, T Wirtavuori, K Hakkinen, AM Flint, J
Citation: P. Nokelainen et al., Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: An inherited encephalopathy of childhood?, AM J MED G, 103(3), 2001, pp. 198-206

Authors: Nokelainen, P Peltoketo, H Mustonen, M Vihko, P
Citation: P. Nokelainen et al., Expression of mouse 17 beta-hydroxysteroid dehydrogenase/17-ketosteroid reductase type 7 in the ovary, uterus, and placenta: Localization from implantation to late pregnancy, ENDOCRINOL, 141(2), 2000, pp. 772-778

Authors: Nokelainen, P Heiskala, H Lehesjoki, AE Kaski, M
Citation: P. Nokelainen et al., A patient with 2 different repeat expansion mutations, ARCH NEUROL, 57(8), 2000, pp. 1199-1203

Authors: Peltoketo, H Nokelainen, P Piao, YS Vihko, R Vihko, P
Citation: H. Peltoketo et al., Two 17 beta-hydroxysteroid dehydrogenases (17HSDs) of estradiol biosynthesis: 17HSD type 1 and type 7, J STEROID B, 69(1-6), 1999, pp. 431-439
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