Showing results (1-10 of 85) with videos related to
Sort By:
Pageof 9
Journal of Medical Genetics|February 5, 2002
Preimplantation genetic diagnosis in clinical practiceE Kanavakis, J Traeger-SynodinosHuman Genetics|January 26, 2002
Qualitative and quantitative analysis of mRNA associated with four putative splicing mutations (621+3A-->G, 2751+2T-->A, 296+1G-->C, 1717-9T-->C-D565G) and one nonsense mutation (E822X) in the CFTR geneM Tzetis, A Efthymiadou, S Doudounakis, et al.Pediatric Hematology and Oncology|July 1, 1997
Tissue oxygenation in patients with hemoglobinopathy HI Papassotiriou, E Kanavakis, A Stamoulakatou, et al.British Journal of Haematology|June 1, 1986
The molecular basis of HbH disease in GreeceS Tzotzos, E Kanavakis, A Metaxotou-Mavromati, et al.American Journal of Hematology|July 1, 1986
Frequency of alpha-thalassemia in GreeceE Kanavakis, S Tzotzos, A Liapaki, et al.American Journal of Hematology|November 1, 1993
Characterization of nondeletion alpha-thalassemia mutations in the Greek populationJ Traeger-Synodinos, E Kanavakis, M Tzetis, et al.Genetic Counseling (Geneva, Switzerland)|November 21, 2007
Saethre-Chotzen syndrome with severe developmental delay associated with deletion of chromosomic region 7p15 --> pterV Touliatou, A Mavrou, A Kolialexi, et al.Lancet (London, England)|February 27, 1988
Correlation of clinical phenotype to genotype in haemoglobin H diseaseC Kattamis, S Tzotzos, E Kanavakis, et al.Journal of Medical Genetics|March 1, 1988
Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemiaA Metaxotou-Mavromati, C Kattamis, L Matathia, et al.Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Clinical manifestations in 17 Greek patients with Goldenhar syndromeV Touliatou, H Fryssira, A Mavrou, et al.Pageof 9