Authors: Velissariou, V Antoniadi, T Patsalis, P Christopoulou, S Hatzipouliou, A Donoghue, J Bakou, K Kaminopetros, P Athanassiou, V Petersen, MB

Citation: V. Velissariou et al., Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis, PRENAT DIAG, 21(6), 2001, pp. 484-487

Authors: Antoniadi, T Pampanos, A Petersen, MB

Citation: T. Antoniadi et al., Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation, PRENAT DIAG, 21(1), 2001, pp. 10-13

Authors: Antoniadi, T Gronskov, K Sand, A Pampanos, A Brondum-Nielsen, K Petersen, MB

Citation: T. Antoniadi et al., Mutation analysis of the GJB2 (Connexin 26) gene by DGGE in Greek patientswith sensorineural deafness, HUM MUTAT, 16(1), 2000, pp. 7-12

Authors: Antoniadi, T Hatzis, T Kroupis, C Economou-Petersen, E Petersen, MB

Citation: T. Antoniadi et al., Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors, AM J HEMAT, 61(4), 1999, pp. 265-267

Authors: Vrettou, C Palmer, G Kanavakis, E Tzetis, M Antoniadi, T Mastrominas, M Traeger-Synodinos, J

Citation: C. Vrettou et al., A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: Application to preimplantation genetic diagnosis, PRENAT DIAG, 19(13), 1999, pp. 1209-1216

Authors: Antoniadi, T Rabionet, R Kroupis, C Aperis, GA Economides, J Petmezakis, J Economou-Petersen, E Estivill, X Petersen, MB

Citation: T. Antoniadi et al., High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness, CLIN GENET, 55(5), 1999, pp. 381-382