Authors: Horvath, A Savov, A Kirov, S Karshelova, E Paskaleva, I Goudev, A Ganev, V

Citation: A. Horvath et al., High frequency of the ApoB-100 R3500Q mutation in Bulgarian hypercholesterolaemic subjects, J MED GENET, 38(8), 2001, pp. 536-540

Authors: Chandler, D Angelicheva, D Heather, L Gooding, R Gresham, D Yanakiev, P de Jonge, R Baas, F Dye, D Karagyozov, L Savov, A Blechschmidt, K Keats, B Thomas, PK King, RHM Starr, A Nikolova, A Colomer, J Ishpekova, B Tournev, I Urtizberea, JA Merlini, L Butinar, D Chabrol, B Voit, T Baethmann, M Nedkova, V Corches, A Kalaydjieva, L

Citation: D. Chandler et al., Hereditary motor and sensory neuropathy Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries, NEUROMUSC D, 10(8), 2000, pp. 584-591

Authors: Kilinc, MO Ninis, VN Tolun, A Estivill, X Casals, T Savov, A Dagli, E Karakoc, F Demirkol, M Huner, G Ozkinay, F Demir, E Seculi, JL Pena, J Bousono, C Ferrer-Calvete, J Calvo, C Glover, G Kremenski, I

Citation: Mo. Kilinc et al., Genotype-phenotype correlation in three homozygotes and nine compound heterozygotes for the cystic fibrosis mutation 2183AA -> G shows a severe phenotype, J MED GENET, 37(4), 2000, pp. 307-309

Authors: Kalaydjieva, L Perez-Lezaun, A Angelicheva, D Onengut, S Dye, D Bosshard, NU Jordanova, A Savov, A Yanakiev, P Kremensky, I Radeva, B Hallmayer, J Markov, A Nedkova, V Tournev, I Aneva, L Gitzelmann, R

Citation: L. Kalaydjieva et al., A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies), AM J HU GEN, 65(5), 1999, pp. 1299-1307

Authors: Demirov, D Savov, A Kremensky, I Ganev, V

Citation: D. Demirov et al., A screening approach for selection of clones simultaneously mutagenized atmultiple sites, ANALYT BIOC, 265(2), 1998, pp. 384-386