Your search returned 22 results.

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	1.	[DNA diagnosis of muscular dystrophies]. [electronic resource] by Lindlöf, M Somer, H Producer: 19890314 In: Duodecim; laaketieteellinen aikakauskirja vol. 104 Availability: No items available. Save to lists Add to cart (remove)
	2.	Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy. [electronic resource] by Lindlöf, M Sistonen, P de la Chapelle, A Producer: 19880513 In: Annals of human genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	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)
	4.	Carrier testing of children for two X-linked diseases: A retrospective study of comprehension of the test results and social and psychological significance of the testing. [electronic resource] by Järvinen, O Lehesjoki, A E Lindlöf, M Uutela, A Kääriäinen, H Producer: 20001214 In: Pediatrics vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Karyotype and BCR studies after bone marrow transplantation for chronic myeloid leukaemia. [electronic resource] by Ruutu, T Peltomäki, P Volin, L Lindlöf, M Knuutila, S Producer: 19910927 In: Bone marrow transplantation vol. 7 Suppl 2 Availability: No items available. Save to lists Add to cart (remove)
	6.	Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results. [electronic resource] by Kääriäinen, H Lindlöf, M Somer, H de la Chapelle, A Producer: 19900516 In: Clinical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms. [electronic resource] by Lindlöf, M Kääriäinen, H Davies, K E de la Chapelle, A Producer: 19870311 In: Journal of medical genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Carrier testing of children for two X-linked diseases: a retrospective evaluation of experience and satisfaction of subjects and their mothers. [electronic resource] by Järvinen, O Lehesjoki, A E Lindlöf, M Uutela, A Kääriäinen, H Producer: 20000127 In: Genetic testing vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Lymphocytic beta-adrenergic receptors in X-linked muscular dystrophy. [electronic resource] by Mäki, T Somer, H Pihko, H Lindlöf, M Kontula, K Härkönen, M Producer: 19891201 In: Journal of the neurological sciences vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations. [electronic resource] by Lindlöf, M Kääriäinen, H van Ommen, G J de la Chapelle, A Producer: 19880527 In: Clinical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis. [electronic resource] by de la Chapelle, A Sankila, E M Lindlöf, M Aula, P Norio, R Producer: 19860102 In: Clinical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Combined RT-PCR and metaphase-FISH posttransplant studies in pediatric patients with chronic myeloid leukemia. [electronic resource] by Vettenranta, K Huhta, T Lindlöf, M Knuutila, S Saarinen-Pihkala, U M Producer: 19980429 In: Journal of pediatric hematology/oncology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Philadelphia chromosome as the sole abnormality and p210 bcr-abl chimeric protein expression in an Epstein-Barr virus-transformed B cell line from a patient with chronic myeloid leukemia. [electronic resource] by Knuutila, S Lindlöf, M Kovanen, P E Ramqvist, T Ruutu, T Andersson, L C Producer: 19940428 In: Acta haematologica vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Carrier testing of children for two X linked diseases in a family based setting: a retrospective long term psychosocial evaluation. [electronic resource] by Järvinen, O Aalto, A M Lehesjoki, A E Lindlöf, M Söderling, I Uutela, A Kääriäinen, H Producer: 19990927 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	15.	[Diagnosis of Duchenne's muscular dystrophy using recombinant DNA technics]. [electronic resource] by Lindlöf, M Ammälä, P Somer, H Somer, M Simola, K O de la Chapelle, A Producer: 19860220 In: Duodecim; laaketieteellinen aikakauskirja vol. 101 Availability: No items available. Save to lists Add to cart (remove)
	16.	Erythropoietin receptor mutations associated with familial erythrocytosis cause hypersensitivity to erythropoietin in the heterozygous state. [electronic resource] by Watowich, S S Xie, X Klingmuller, U Kere, J Lindlof, M Berglund, S de la Chapelle, A Producer: 19991104 In: Blood vol. 94 Availability: No items available. Save to lists Add to cart (remove)
	17.	Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis. [electronic resource] by Ikonen, R S Lindlöf, M Janas, M O Simola, K O Millington-Ward, A de la Chapelle, A Producer: 19891116 In: Human genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Prenatal diagnosis of X-linked chronic granulomatous disease using restriction fragment length polymorphism analysis. [electronic resource] by Lindlöf, M Kere, J Ristola, M Repo, H Leirisalo-Repo, M von Koskull, H Ammälä, P de la Chapelle, A Producer: 19871214 In: Genomics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Gene deletions in X-linked muscular dystrophy. [electronic resource] by Lindlöf, M Kiuru, A Kääriäinen, H Kalimo, H Lang, H Pihko, H Rapola, J Somer, H Somer, M Savontaus, M L Producer: 19890503 In: American journal of human genetics vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	20.	Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq. [electronic resource] by Saviranta, P Lindlöf, M Lehesjoki, A E Kalimo, H Lang, H Sonninen, V Savontaus, M L de la Chapelle, A Producer: 19880223 In: American journal of human genetics vol. 42 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 22 results.