Rare Case of a Heterozygous Microdeletion 9q21.11-q21.2: Clinical and Genetic Characteristics

por Ivanov, HY, Stoyanova, V, Ivanov, I, Linev, A, Vazharova, R, Ivanov, S, Balabanski, L, Toncheva, D
Publicado 2018

NGS Nominated CELA1, HSPG2, and KCNK5 as Candidate Genes for Predisposition to Balkan Endemic Nephropathy

por Toncheva, D., Mihailova-Hristova, M., Vazharova, R., Staneva, R., Karachanak, S., Dimitrov, P., Simeonov, V., Ivanov, S., Balabanski, L., Serbezov, D., Malinov, M., Stefanovic, V., Čukuranović, R., Polenakovic, M., Jankovic-Velickovic, L., Djordjevic, V., Jevtovic-Stoimenov, T., Plaseska-Karanfilska, D., Galabov, A., Djonov, V., Dimova, I.
Publicado 2014