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	1.	A Finnish BRCA1 exon 12 4216-2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation. [electronic resource] by Hartikainen, J M Pirskanen, M M Arffman, A H Ristonmaa, U K Mannermaa, A J Producer: 20000120 In: Human mutation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Insertion-deletion polymorphism in the gene for angiotensin-converting enzyme is associated with obstetric cholestasis but not with preeclampsia. [electronic resource] by Heiskanen, J T Pirskanen, M M Hiltunen, M J Mannermaa, A J Punnonen, K R Heinonen, S T Producer: 20011011 In: American journal of obstetrics and gynecology vol. 185 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Molecular genetic analysis of the alpha-synuclein and the parkin gene in Parkinson's disease in Finland. [electronic resource] by Autere, J M Hiltunen, M J Mannermaa, A J Jäkälä, P A Hartikainen, P H Majamaa, K Alafuzoff, I Soininen, H S Producer: 20021126 In: European journal of neurology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Failure in post-transcriptional processing is a possible inactivation mechanism of AP-2alpha in cutaneous melanoma. [electronic resource] by Karjalainen, J M Kellokoski, J K Mannermaa, A J Kujala, H E Moisio, K I Mitchell, P J Eskelinen, M J Alhava, E M Kosma, V M Producer: 20000710 In: British journal of cancer vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)