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	21.	DXS26 (HU16) is located in Xq21.1. [electronic resource] by Sankila, E M Bruns, G A Schwartz, M Nikoskelainen, E Niebuhr, E Hodgson, S V Wright, A F de la Chapelle, A Producer: 19900801 In: Human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Autosomal recessive cornea plana: in vivo corneal morphology and corneal sensitivity. [electronic resource] by Vesaluoma, M H Sankila, E M Gallar, J Müller, L J Petroll, W M Moilanen, J A Forsius, H Tervo, T M Producer: 20000731 In: Investigative ophthalmology & visual science vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	23.	Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase. [electronic resource] by Murphy, D L Sims, K B Karoum, F Garrick, N A de la Chapelle, A Sankila, E M Norio, R Breakefield, X O Producer: 19910528 In: Journal of neural transmission. General section vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients. [electronic resource] by Plantinga, R F Kleemola, L Huygen, P L M Joensuu, T Sankila, E-M Pennings, R J E Cremers, C W R J Producer: 20050926 In: Audiology & neuro-otology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Norrie disease gene is distinct from the monoamine oxidase genes. [electronic resource] by Sims, K B Ozelius, L Corey, T Rinehart, W B Liberfarb, R Haines, J Chen, W J Norio, R Sankila, E de la Chapelle, A Producer: 19890922 In: American journal of human genetics vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	26.	Anti-clarin-1 AAV-delivered ribozyme induced apoptosis in the mouse cochlea. [electronic resource] by Aarnisalo, A A Pietola, L Joensuu, J Isosomppi, J Aarnisalo, P Dinculescu, A Lewin, A S Flannery, J Hauswirth, W W Sankila, E-M Jero, J Producer: 20070919 In: Hearing research vol. 230 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients. [electronic resource] by van Bokhoven, H Schwartz, M Andréasson, S van den Hurk, J A Bogerd, L Jay, M Rüther, K Jay, B Pawlowitzki, I H Sankila, E M Producer: 19950105 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases. [electronic resource] by Cremers, F P Sankila, E M Brunsmann, F Jay, M Jay, B Wright, A Pinckers, A J Schwartz, M van de Pol, D J Wieringa, B Producer: 19901102 In: American journal of human genetics vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	29.	Monoamine oxidase deficiency in males with an X chromosome deletion. [electronic resource] by Sims, K B de la Chapelle, A Norio, R Sankila, E M Hsu, Y P Rinehart, W B Corey, T J Ozelius, L Powell, J F Bruns, G Producer: 19900406 In: Neuron vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. [electronic resource] by Joensuu, T Hämäläinen, R Yuan, B Johnson, C Tegelberg, S Gasparini, P Zelante, L Pirvola, U Pakarinen, L Lehesjoki, A E de la Chapelle, A Sankila, E M Producer: 20011018 In: American journal of human genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3. [electronic resource] by Bitner-Glindzicz, M Turnpenny, P Höglund, P Kääriäinen, H Sankila, E M van der Maarel, S M de Kok, Y J Ropers, H H Cremers, F P Pembrey, M Producer: 19951215 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia. [electronic resource] by Cremers, F P van de Pol, D J Wieringa, B Collins, F S Sankila, E M Siu, V M Flintoff, W F Brunsmann, F Blonden, L A Ropers, H H Producer: 19891109 In: Proceedings of the National Academy of Sciences of the United States of America vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. [electronic resource] by Aittomäki, K Lucena, J L Pakarinen, P Sistonen, P Tapanainen, J Gromoll, J Kaskikari, R Sankila, E M Lehväslaiho, H Engel, A R Nieschlag, E Huhtaniemi, I de la Chapelle, A Producer: 19951027 In: Cell vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)