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	1.	Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosis. [electronic resource] by de la Chapelle, A Träskelin, A L Juvonen, E Producer: 19930702 In: Proceedings of the National Academy of Sciences of the United States of America vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic mapping of the erythropoietin receptor gene. [electronic resource] by Sistonen, P Träskelin, A L Lehväslaiho, H de la Chapelle, A Producer: 19931117 In: Human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mapping of the regulatory subunits RI beta and RII beta of cAMP-dependent protein kinase genes on human chromosome 7. [electronic resource] by Solberg, R Sistonen, P Träskelin, A L Bérubé, D Simard, J Krajci, P Jahnsen, T de la Chapelle, A Producer: 19921222 In: Genomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q. [electronic resource] by Virtaneva, K Miao, J Träskelin, A L Stone, N Warrington, J A Weissenbach, J Myers, R M Cox, D R Sistonen, P de la Chapelle, A Producer: 19960725 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	5.	Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome. [electronic resource] by Balikova, I Lehesjoki, A-E de Ravel, T J L Thienpont, B Chandler, K E Clayton-Smith, J Träskelin, A-L Fryns, J-P Vermeesch, J R Producer: 20091117 In: Human mutation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)