Whole Genome Analysis by Array-Based Comparative Genomic Hybridization in Patients with Congenital Malformations
Dimova, I, Vazharova, R, Nikolova, D, Tincheva, R, Nesheva, D, Uzunova, Y, Toncheva, D
Array-Based Comparative Genomic Hybridization Application for Revealing Genomic Micro Imbalances in Congenital Malformations
Hadjidekova, S, Toncheva, D
Web-Based Software for Storage, Statistical Processing and Analysis of SNP Data in Studies on Complex Disorders
Betcheva, E, Betchev, C, Toncheva, D
Copy Number Changes in 1q21.3 and 1q23.3 have Different Clinical Relevance in Ovarian Tumors
Dimova, I, Orsetti, B, Theillet, Ch., Dimitrov, R., Toncheva, D
Chromatin Quality as a Crucial Factor for the Success of Fluorescent in Situ Hybridization Analyses of Unfertilized Oocytes, Polar Bodies and Arrested Zygotes
Zhivkova, R, Delimitreva, S, Toncheva, D, Vatev, I
Apoptosis Gene Expression Profile in Early-Stage non Small Cell Lung Cancer
Metodieva, S, Cherneva, R, Nikolova, D, Genchev, G, Petrov, D, Toncheva, D
Epigenetic alterations in patients with type 2 diabetes mellitus
Karachanak-Yankova, S, Dimova, R, Nikolova, D, Nesheva, D, Koprinarova, M, Maslyankov, S, Tafradjiska, R, Gateva, P, Velizarova, M, Hammoudeh, Z, Stoynev, N, Toncheva, D, Tankova, T, Dimova, I
Benign, pathogenic and copy number variations of unknown clinical significance in patients with congenital malformations and developmental delay
Mihaylova, M, Staneva, R, Toncheva, D, Pancheva, M, Hadjidekova, S
Detecting EGFR mutations in patients with non-small cell lung cancer
Hammoudeh, ZA, Antonova, O, Staneva, R, Nikolova, D, Kyuchukov, Y, Penev, A, Mintchev, T, Koleva, V, Hadjidekova, S, Toncheva, D
Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics
Ivanov, HY, Stoyanova, V, Ivanov, I, Linev, A, Vazharova, R, Ivanov, S, Balabanski, L, Toncheva, D
Janus kinase V617F mutation detection in patients with myelofibrosis
Nikolova, D, Yordanov, A, Damyanova, V, Radinov, A, Toncheva, D