S. Ivanov

发表

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

D. Toncheva, Ivanov Hy, Stoyanova V, 2018, Balkan journal of medical genetics : BJMG.

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

D. Toncheva, R. Vazharova, S. Ivanov, 2017 .

NGS Nominated CELA 1 , HSPG 2 , and KCNK 5 as Candidate Genes for Predisposition to Balkan Endemic Nephropathy

D. Toncheva, D. Plaseska-Karanfilska, R., 2014 .

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

D. Toncheva, D. Plaseska-Karanfilska, P. Dimitrov, 2014, BioMed research international.

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

D. Toncheva, I. Ivanov, R. Vazharova, 2018, Biotechnology & Biotechnological Equipment.

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

D. Toncheva, V. Stoyanova, I. Ivanov, 2015 .

Genetic, Genomic and Epigenomic Studies of Balkan Endemic Nephropathy (Ben)

D. Toncheva, P. Dimitrov, M. Polenaković, 2015, Prilozi.

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

D. Toncheva, R. Vazharova, S. Ivanov, 2016, Case reports in obstetrics and gynecology.

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

D. Toncheva, R. Vazharova, S. Ivanov, 2016, memo - Magazine of European Medical Oncology.

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

D. Toncheva, D. Nesheva, S. Ivanov, 2014, Molecular and clinical oncology.

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

D. Toncheva, D. Nesheva, S. Ivanov, 2014, Molecular and clinical oncology.