Search Results - Vazharova, R.

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  1. 1
    APC promoter 1B deletion in familial polyposis-implications for mutation-negative families

    APC promoter 1B deletion in familial polyposis-implications for mutation-negative families by Kadiyska, T.K., Todorov, T.P., Bichev, S.N., Vazharova, R.V., Nossikoff, A.V., Savov, A.S., Mitev, V.I.

    Published in Clinical genetics
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  2. 2
    Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics

    Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics by Ivanov, HY, Stoyanova, V, Ivanov, I, Linev, A, Vazharova, R, Ivanov, S, Balabanski, L, Toncheva, D

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  3. 3
    Genome‐wide association study on bipolar disorder in the Bulgarian population

    Genome‐wide association study on bipolar disorder in the Bulgarian population by Yosifova, A., Mushiroda, T., Kubo, M., Takahashi, A., Kamatani, Y., Kamatani, N., Stoianov, D., Vazharova, R., Karachanak, S., Zaharieva, I., Dimova, I., Hadjidekova, S., Milanova, V., Madjirova, N., Gerdjikov, I., Tolev, T., Poryazova, N., O'Donovan, M. C., Owen, M. J., Kirov, G., Toncheva, D., Nakamura, Y.

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  4. 4
    NGS Nominated CELA1, HSPG2, and KCNK5 as Candidate Genes for Predisposition to Balkan Endemic Nephropathy

    NGS Nominated CELA1, HSPG2, and KCNK5 as Candidate Genes for Predisposition to Balkan Endemic Nephropathy by Dimitrov, P., Karachanak, S., Staneva, R., Vazharova, R., Mihailova-Hristova, M., Toncheva, D., Simeonov, V., Ivanov, S., Balabanski, L., Serbezov, D., Malinov, M., Stefanovic, Vladisav, Čukuranović, Rade, Polenakovic, M., Jankovic-Velickovic, Ljubinka, Djordjević, Vidosava B., Jevtovic-Stoimenov, T., Plaseska-Karanfilska, D., Galabov, A., Djonov, V., Dimova, I.

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  5. 5
    Whole Genome Analysis by Array-Based Comparative Genomic Hybridization in Patients with Congenital Malformations

    Whole Genome Analysis by Array-Based Comparative Genomic Hybridization in Patients with Congenital Malformations by Dimova, I, Vazharova, R, Nikolova, D, Tincheva, R, Nesheva, D, Uzunova, Y, Toncheva, D

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  6. 6
    TruSight Cancer Sequencing Panel reveals pharmacogenetic variants associated with sensitivity to chemotherapy in lung cancer

    TruSight Cancer Sequencing Panel reveals pharmacogenetic variants associated with sensitivity to chemotherapy in lung cancer by Chilingirova, N., Hammoudeh, Z., Balabanski, L., Ivanov, S., Vazharova, R., Nikolova, D., Kurteva, G., Toncheva, D., Chilingirov, P.

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  7. 7
    Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria-estimation of applicability of 6 STR markers on chromosomes 21 and 18

    Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria-estimation of applicability of 6 STR markers on chromosomes 21 and 18 by Andonova, Silvia, Vazharova, Radoslava, Dimitrova, Violeta, Mazneikova, Valentina, Toncheva, Draga, Kremensky, Ivo

    Published in Prenatal diagnosis
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