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	1.	Genetic effects on human cognition: lessons from the study of mental retardation syndromes. [electronic resource] by Nokelainen, P Flint, J Producer: 20020328 In: Journal of neurology, neurosurgery, and psychiatry vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Expression cloning of a novel estrogenic mouse 17 beta-hydroxysteroid dehydrogenase/17-ketosteroid reductase (m17HSD7), previously described as a prolactin receptor-associated protein (PRAP) in rat. [electronic resource] by Nokelainen, P Peltoketo, H Vihko, R Vihko, P Producer: 19981005 In: Molecular endocrinology (Baltimore, Md.) vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Expression of mouse 17beta-hydroxysteroid dehydrogenase/17-ketosteroid reductase type 7 in the ovary, uterus, and placenta: localization from implantation to late pregnancy. [electronic resource] by Nokelainen, P Peltoketo, H Mustonen, M Vihko, P Producer: 20000210 In: Endocrinology vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Linkage analyses in tibial muscular dystrophy. [electronic resource] by Nokelainen, P Udd, B Somer, H Peltonen, L Producer: 19960805 In: Human heredity vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A patient with 2 different repeat expansion mutations. [electronic resource] by Nokelainen, P Heiskala, H Lehesjoki, A E Kaski, M Producer: 20000906 In: Archives of neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy. [electronic resource] by Udd, B Rapola, J Nokelainen, P Arikawa, E Somer, H Producer: 19930224 In: Journal of the neurological sciences vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Evaluation of the ARKRAY AUTION Eleven reflectometer in detecting microalbuminuria with AUTION Screen test strips and proteinuria with AUTION Sticks 10PA strips. [electronic resource] by Kouri, T Nokelainen, P Pelkonen, V Kosaka, H Saeger, B Producer: 20090320 In: Scandinavian journal of clinical and laboratory investigation vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Two 17beta-hydroxysteroid dehydrogenases (17HSDs) of estradiol biosynthesis: 17HSD type 1 and type 7. [electronic resource] by Peltoketo, H Nokelainen, P Piao, Y S Vihko, R Vihko, P Producer: 19990802 In: The Journal of steroid biochemistry and molecular biology vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Molecular cloning of mouse 17 beta-hydroxysteroid dehydrogenase type 1 and characterization of enzyme activity. [electronic resource] by Nokelainen, P Puranen, T Peltoketo, H Orava, M Vihko, P Vihko, R Producer: 19960603 In: European journal of biochemistry vol. 236 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	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? [electronic resource] by Nokelainen, P Heiskala, H Raininko, R Autti, T Wirtavuori, K Häkkinen, A M Flint, J Producer: 20020214 In: American journal of medical genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy. [electronic resource] by Nokelainen, P T Alanen-Kurki, L Somer, H V Pihko, S H Peltonen, L Producer: 19910916 In: Muscle & nerve vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Rat 17 beta-hydroxysteroid dehydrogenase type 1: primary structure and regulation of enzyme expression in rat ovary by diethylstilbestrol and gonadotropins in vivo. [electronic resource] by Ghersevich, S Nokelainen, P Poutanen, M Orava, M Autio-Harmainen, H Rajaniemi, H Vihko, R Producer: 19941024 In: Endocrinology vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicine. [electronic resource] by Sajantila, A Pacek, P Lukka, M Syvänen, A C Nokelainen, P Sistonen, P Peltonen, L Budowle, B Producer: 19950111 In: Forensic science international vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations. [electronic resource] by Davies, J Yamagata, H Shelbourne, P Buxton, J Ogihara, T Nokelainen, P Nakagawa, M Williamson, R Johnson, K Miki, T Producer: 19930107 In: Journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population. [electronic resource] by Nokelainen, P Alanen-Kurki, L Winqvist, R Falck, B Somer, H Leisti, J Johnson, K Savontaus, M L Peltonen, L Producer: 19901205 In: Human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Meiotic drive at the myotonic dystrophy locus? [electronic resource] by Carey, N Johnson, K Nokelainen, P Peltonen, L Savontaus, M L Juvonen, V Anvret, M Grandell, U Chotai, K Robertson, E Producer: 19940525 In: Nature genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	The DM mutation; diagnostic applications in the Finnish population. [electronic resource] by Nokelainen, P Shelbourne, P Shaw, D Brook, J D Harley, H G Johnson, K Somer, H Savontaus, M L Peltonen, L Producer: 19930816 In: Clinical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)