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	1.	Population cytogenetics of folate-sensitive fragile sites. I. Common fragile sites. [electronic resource] by Kähkönen, M Producer: 19890118 In: Human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A molecular and cytogenetic study in Finnish Prader-Willi patients. [electronic resource] by Kokkonen, H Kähkönen, M Leisti, J Producer: 19950627 In: Human genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Notable chromosomal anomalies in a woman receiving drugs during the period of viremia after rubella vaccination. [electronic resource] by Knuutila, S Kähkönen, M Wilska, M Producer: 19770331 In: Hereditas vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Uridine enhances expression of the fragile X chromosome in human lymphocytes. [electronic resource] by Kähkönen, M Haataja, R Leisti, J Producer: 19910702 In: Human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Fanconi's anaemia; chromosome breakage in a large African family. [electronic resource] by Meme, J S Greipenberg, U Kähkönen, M Producer: 19810226 In: Hereditas vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[X-chromosome-linked mental deficiency and the chromosome marker fra(X)(q28)]. [electronic resource] by Simola, K O Kähkönen, M Leisti, J Producer: 19820814 In: Duodecim; laaketieteellinen aikakauskirja vol. 98 Availability: No items available. Save to lists Add to cart (remove)
	7.	Diagnosis of fragile X syndrome by direct mutation analysis. [electronic resource] by Väisänen, M L Kähkönen, M Leisti, J Producer: 19940329 In: Human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis. [electronic resource] by Väisänen, M L Kähkönen, M Leisti, J Producer: 19920716 In: American journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Marker X-associated mental retardation. A study of 150 retarded males. [electronic resource] by Kähkönen, M Leisti, J Wilska, M Varonen, S Producer: 19831021 In: Clinical genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Chromosomal abnormalities in relation to clinical disease in patients with cutaneous T-cell lymphoma: a 5-year follow-up study. [electronic resource] by Karenko, L Sarna, S Kähkönen, M Ranki, A Producer: 20030319 In: The British journal of dermatology vol. 148 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Berry phenolics and their antioxidant activity. [electronic resource] by Kähkönen, M P Hopia, A I Heinonen, M Producer: 20011204 In: Journal of agricultural and food chemistry vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Diamniotic omphalopagus conjoined twins in a diamniotic pregnancy. [electronic resource] by Tihtonen, K Lagerstedt, A Kähkönen, M Kirkinen, P Producer: 20091203 In: Fetal diagnosis and therapy vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	An increased frequency of chromosomal changes and SCE's in cultured blood lymphocytes of 12 subjects vaccinated against smallpox. [electronic resource] by Knuutila, S Mäki-Paakkanen, J Kähkönen, M Hokkanen, E Producer: 19780508 In: Human genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	[X-linked lymphoproliferative syndrome]. [electronic resource] by Pelkonen, T Lanning, M Kähkönen, M Gross, T G Producer: 20001016 In: Duodecim; laaketieteellinen aikakauskirja vol. 112 Availability: No items available. Save to lists Add to cart (remove)
	15.	Frequency of rare fragile sites among mentally subnormal schoolchildren. [electronic resource] by Kähkönen, M Leisti, J Thoden, C J Autio, S Producer: 19870122 In: Clinical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Mutagenicity of Bacillus thuringiensis exotoxin III. Sister chromatid exchange in rats in vivo. [electronic resource] by Kähkönen, M Gripenberg, U Carlberg, G Meretoja, T Sorsa, M Producer: 19800128 In: Hereditas vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	A chromosome survey of 1062 mentally retarded patients. Evaluation of a long-term study at the Rinnekoti institution, Finland. [electronic resource] by Gripenberg, U Hongell, K Knuutila, S Kähkönen, M Leisti, J Producer: 19800926 In: Hereditas vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Partial trisomy 12q: clinical and cytogenetic observations. [electronic resource] by Tengström, C Wilska, M Kähkönen, M Autio, S Leisti, J Producer: 19851119 In: Clinical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Notable losses at specific regions of chromosomes 10q and 13q in the Sézary syndrome detected by comparative genomic hybridization. [electronic resource] by Karenko, L Kähkönen, M Hyytinen, E R Lindlof, M Ranki, A Producer: 19990413 In: The Journal of investigative dermatology vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations. [electronic resource] by Dostal, A Linnankivi, T Somer, M Kähkönen, M Litzman, J Tienari, P Producer: 20070730 In: International journal of immunogenetics vol. 34 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 40 results.