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Human 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.

Revista Argentina De Microbiologia|January 14, 2011

Anton van Leeuwenhoek (1632-1723): father of micromorphology and discoverer of spermatozoaM Karamanou, E Poulakou-Rebelakou, M Tzetis, 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.

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.

Molecular Human Reproduction|June 10, 1998

Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermiaE Kanavakis, M Tzetis, T Antoniadi, et al.

British Journal of Haematology|October 1, 1991

The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalenceJ Traeger-Synodinos, M Tzetis, E Kanavakis, et al.

Human Genetics|January 1, 1997

Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutationsM Tzetis, E Kanavakis, T Antoniadi, et al.

Hematologic Pathology|January 1, 1994

The molecular basis of normal HbA2 (type 2) beta-thalassemia in GreeceM Tzetis, J Traeger-Synodinos, E Kanavakis, et al.

Prenatal Diagnosis|February 8, 2000

Preimplantation genetic diagnosis in 10 couples at risk for transmitting beta-thalassaemia major: clinical experience including the initiation of six singleton pregnanciesE Kanavakis, C Vrettou, G Palmer, et al.

Clinical Genetics|May 20, 2003

Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individualsE Kanavakis, A Efthymiadou, S Strofalis, et al.

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Showing results (1-10 of 36) with videos related to

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Human 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.

Revista Argentina De Microbiologia|January 14, 2011

Anton van Leeuwenhoek (1632-1723): father of micromorphology and discoverer of spermatozoaM Karamanou, E Poulakou-Rebelakou, M Tzetis, 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.

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.

Molecular Human Reproduction|June 10, 1998

Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermiaE Kanavakis, M Tzetis, T Antoniadi, et al.

British Journal of Haematology|October 1, 1991

The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalenceJ Traeger-Synodinos, M Tzetis, E Kanavakis, et al.

Human Genetics|January 1, 1997

Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutationsM Tzetis, E Kanavakis, T Antoniadi, et al.

Hematologic Pathology|January 1, 1994

The molecular basis of normal HbA2 (type 2) beta-thalassemia in GreeceM Tzetis, J Traeger-Synodinos, E Kanavakis, et al.

Prenatal Diagnosis|February 8, 2000

Preimplantation genetic diagnosis in 10 couples at risk for transmitting beta-thalassaemia major: clinical experience including the initiation of six singleton pregnanciesE Kanavakis, C Vrettou, G Palmer, et al.

Clinical Genetics|May 20, 2003

Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individualsE Kanavakis, A Efthymiadou, S Strofalis, et al.

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