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	1.	BARTH SYNDROME IN MALE AND FEMALE SIBLINGS CAUSED BY A NOVEL MUTATION IN THE TAZ GENE. [electronic resource] by Avdjieva-Tzavella, D M Todorova, A P Ivanova, M B Yordanova, I T Todorov, T P Litvinenko, I O Dasheva-Dimitrova, A T Tincheva, R S Producer: 20181016 In: Genetic counseling (Geneva, Switzerland) vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	2.	First Bulgarian case of citrin deficiency caused by one novel and one recurrent mutation in the SLC25A13 gene. [electronic resource] by Avdjieva-Tzavella, D M Ivanova, M B Todorov, T P Todorova, A P Panteleeva, E I Tincheva, S S Lazarova, E A Kathom, H M Yaneva, P G Tincheva, R S Producer: 20141211 In: Genetic counseling (Geneva, Switzerland) vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	3.	Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism. [electronic resource] by Avdjieva-Tzavella, D M Todorov, T P Todorova, A P Kirov, A V Hadjidekova, S P Rukova, B B Litvinenko, I O Hristova-Naydenova, D N Tincheva, R S Toncheva, D I Producer: 20130404 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)

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