Your search returned 27 results.

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	1.	Development of molecular genetics. [electronic resource] by Tahvanainen, E Producer: 19991027 In: Clinical chemistry and laboratory medicine vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Exclusion of two candidate loci for autosomal recessive nemaline myopathy. [electronic resource] by Tahvanainen, E Beggs, A H Wallgren-Pettersson, C Producer: 19940510 In: Journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical features of nine males with molecularly defined deletions of the Y chromosome long arm. [electronic resource] by Salo, P Ignatius, J Simola, K O Tahvanainen, E Kääriäinen, H Producer: 19960213 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Serum phospholipid transfer protein activity and genetic variation of the PLTP gene. [electronic resource] by Tahvanainen, E Jauhiainen, M Funke, H Vartiainen, E Sundvall, J Ehnholm, C Producer: 19991028 In: Atherosclerosis vol. 146 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis. [electronic resource] by Huopaniemi, L Rantala, A Tahvanainen, E de la Chapelle, A Alitalo, T Producer: 19970603 In: American journal of human genetics vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	6.	Autosomal dominant cornea plana: clinical findings in a Cuban family and a review of the literature. [electronic resource] by Sigler-Villanueva, A Tahvanainen, E Lindh, S Dieguez-Lucena, J Forsius, H Producer: 19970916 In: Ophthalmic genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic. [electronic resource] by Ranta, S Pihko, H Santavuori, P Tahvanainen, E de la Chapelle, A Producer: 19950912 In: Neuromuscular disorders : NMD vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in Finland. [electronic resource] by Forsius, H Damsten, M Eriksson, A W Fellman, J Lindh, S Tahvanainen, E Producer: 19980619 In: Acta ophthalmologica Scandinavica vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12. [electronic resource] by Tahvanainen, E Villanueva, A S Forsius, H Salo, P de la Chapelle, A Producer: 19960917 In: Genome research vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Hepatic lipase gene polymorphisms influence plasma HDL levels. Results from Finnish EARS participants. European Atherosclerosis Research Study. [electronic resource] by Murtomäki, S Tahvanainen, E Antikainen, M Tiret, L Nicaud, V Jansen, H Ehnholm, C Producer: 19971120 In: Arteriosclerosis, thrombosis, and vascular biology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	The genetics of cornea plana congenita. [electronic resource] by Tahvanainen, E Forsius, H Kolehmainen, J Damsten, M Fellman, J de la Chapelle, A Producer: 19970512 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Interrelationships between low density lipoprotein receptor defect, serum fatty acid composition, and serum cholesterol concentration. [electronic resource] by Tahvanainen, E Molin, M Laakso, J Sundvall, J Jauhiainen, M Vaskonen, T Karppanen, H Producer: 20050322 In: The Journal of nutritional biochemistry vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage. [electronic resource] by Aminoff, M Tahvanainen, E Gräsbeck, R Weissenbach, J Broch, H de la Chapelle, A Producer: 19951103 In: American journal of human genetics vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	14.	Cholesteryl ester transfer protein gene effect on CETP activity and plasma high-density lipoprotein in European populations. The EARS Group. [electronic resource] by Gudnason, V Kakko, S Nicaud, V Savolainen, M J Kesäniemi, Y A Tahvanainen, E Humphries, S Producer: 19990513 In: European journal of clinical investigation vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Refined mapping of the Cohen syndrome gene by linkage disequilibrium. [electronic resource] by Kolehmainen, J Norio, R Kivitie-Kallio, S Tahvanainen, E de la Chapelle, A Lehesjoki, A E Producer: 19980121 In: European journal of human genetics : EJHG vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	16.	Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis. [electronic resource] by Tahvanainen, E Norio, R Karila, E Ranta, S Weissenbach, J Sistonen, P de la Chapelle, A Producer: 19941109 In: Nature genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Intestinal fatty acid binding protein polymorphism at codon 54 is not associated with postprandial responses to fat and glucose tolerance tests in healthy young Europeans. Results from EARS II participants. [electronic resource] by Tahvanainen, E Molin, M Vainio, S Tiret, L Nicaud, V Farinaro, E Masana, L Ehnholm, C Producer: 20001207 In: Atherosclerosis vol. 152 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	[Linkage and linkage disequilibrium in the Finnish disease heritage]. [electronic resource] by de la Chapelle, A Hästbacka, J Lehesjoki, A E Sulisalo, T Kere, J Tahvanainen, E Sistonen, P Producer: 19960213 In: Duodecim; laaketieteellinen aikakauskirja vol. 110 Availability: No items available. Save to lists Add to cart (remove)
	19.	The Gln-Arg191 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns. [electronic resource] by Antikainen, M Murtomäki, S Syvänne, M Pahlman, R Tahvanainen, E Jauhiainen, M Frick, M H Ehnholm, C Producer: 19961010 In: The Journal of clinical investigation vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis. [electronic resource] by Tahvanainen, E Forsius, H Karila, E Ranta, S Eerola, M Weissenbach, J Sistonen, P de la Chapelle, A Producer: 19950808 In: Genomics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 27 results.