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	1.	Determination of multidrug resistance levels in cultured mammalian cells using ornithine decarboxylase activity. [electronic resource] by Assaraf, Y G Drori, S Bachrach, U Shaugan-Labay, V Producer: 19940418 In: Analytical biochemistry vol. 216 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene. [electronic resource] by Sprecher, E Lestringant, G G Szargel, R Bergman, R Labay, V Frossard, P M Friedman-Birnbaum, R Cohen, N Producer: 19991104 In: The Journal of investigative dermatology vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Atrichia with papular lesions maps to 8p in the region containing the human hairless gene. [electronic resource] by Sprecher, E Bergman, R Szargel, R Raz, T Labay, V Ramon, M Baruch-Gershoni, R Friedman-Birnbaum, R Cohen, N Producer: 19990310 In: American journal of medical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss. [electronic resource] by Labay, V Garrido, G Madeo, A C Nance, W E Friedman, T B Friedman, P L Del Castillo, I Griffith, A J Producer: 20080229 In: Clinical genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA. [electronic resource] by Mandel, H Szargel, R Labay, V Elpeleg, O Saada, A Shalata, A Anbinder, Y Berkowitz, D Hartman, C Barak, M Eriksson, S Cohen, N Producer: 20011207 In: Nature genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. [electronic resource] by Labay, V Raz, T Baron, D Mandel, H Williams, H Barrett, T Szargel, R McDonald, L Shalata, A Nosaka, K Gregory, S Cohen, N Producer: 19990719 In: Nature genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families. [electronic resource] by Raz, T Labay, V Baron, D Szargel, R Anbinder, Y Barrett, T Rabl, W Viana, M B Mandel, H Baruchel, A Cayuela, J M Cohen, N Producer: 20000822 In: Human mutation vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)