Search Results - Ivanov, Samuil

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  1. 1
    SCN8A p.Arg1872Gln mutation in early infantile epileptic encephalopathy type 13: Review and case report

    SCN8A p.Arg1872Gln mutation in early infantile epileptic encephalopathy type 13: Review and case report by Atanasoska, Maya, Vazharova, Radoslava, Ivanov, Ivan, Balabanski, Lubomir, Andonova, Silvia, Ivanov, Samuil, Pacheva, Iliana, Malinov, Maxim, Toncheva, Draga

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  2. 2
    Screening of pharmacogenetic variants associated with drug sensitivity in patients with papillary thyroid carcinoma using next generation sequencing

    Screening of pharmacogenetic variants associated with drug sensitivity in patients with papillary thyroid carcinoma using next generation sequencing by Hammoudeh, Zora, Nikolova, Dragomira, Balabanski, Lubomir, Ivanov, Samuil, Vazharova, Radoslava, Weidner, Sabine, Malinov, Maxim, Toncheva, Draga

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  3. 3
    Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies

    Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies by Toncheva, D., Balabanski, L., Ivanov, S., Dimitrova, Violeta, Vragaleva, Svetlana, Vazharova, Radoslava, Malinov, Maxim

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    A de novo microdeletion 2p24.3-25.1 identified in a girl with global development delay

    A de novo microdeletion 2p24.3-25.1 identified in a girl with global development delay by Ivanov, Hristo Y., Stoyanova, Vili K., Vazharova, Radoslava, Linev, Aleksandar, Ivanov, Ivan, Ivanov, Samuil, Balabanski, Lubomir, Toncheva, Draga

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  5. 5
    Next-generation sequencing of BRCA1 and BRCA2 in breast cancer patients and control subjects

    Next-generation sequencing of BRCA1 and BRCA2 in breast cancer patients and control subjects by BALABANSKI, LUBOMIR, ANTOV, GEORGI, DIMOVA, IVANKA, IVANOV, SAMUIL, NACHEVA, MARIA, GAVRILOV, IVAN, NESHEVA, DESISLAVA, RUKOVA, BLAGA, HADJIDEKOVA, SAVINA, MALINOV, MAXIM, TONCHEVA, DRAGA

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