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	1.	Seborrhoeic keratosis removal in a multicentre phase I/II clinical trial using a novel topical formulation (BL-5010). [electronic resource] by Levy-Nissenbaum, E Thio, H B Burstein, P Thaci, D Producer: 20160412 In: The British journal of dermatology vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family. [electronic resource] by Pras, E Frydman, M Levy-Nissenbaum, E Bakhan, T Raz, J Assia, E I Goldman, B Pras, E Producer: 20001012 In: Investigative ophthalmology & visual science vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	3.	Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneity. [electronic resource] by Levy-Nissenbaum, E Eldar, M Wang, Q Lahat, H Belhassen, B Ries, L Friedman, E Pras, E Producer: 20020515 In: Genetic testing vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21. [electronic resource] by Lahat, H Eldar, M Levy-Nissenbaum, E Bahan, T Friedman, E Khoury, A Lorber, A Kastner, D L Goldman, B Pras, E Producer: 20010719 In: Circulation vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A gene causing autosomal recessive cataract maps to the short arm of chromosome 3. [electronic resource] by Pras, E Pras, E Bakhan, T Levy-Nissenbaum, E Lahat, H Assia, E I Garzozi, H J Kastner, D L Goldman, B Frydman, M Producer: 20010906 In: The Israel Medical Association journal : IMAJ vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	6.	A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. [electronic resource] by Lahat, H Pras, E Olender, T Avidan, N Ben-Asher, E Man, O Levy-Nissenbaum, E Khoury, A Lorber, A Goldman, B Lancet, D Eldar, M Producer: 20020110 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)