Tzetis M - Search Results

1

Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype.

Giannikou K, Fryssira H, Oikonomakis V, Syrmou A, Kosma K, Tzetis M, Kitsiou-Tzeli S, Kanavakis E. Giannikou K, et al. Among authors: tzetis m. Gene. 2012 Sep 15;506(2):360-8. doi: 10.1016/j.gene.2012.06.060. Epub 2012 Jul 2. Gene. 2012. PMID: 22766398

2

The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalence.

Traeger-Synodinos J, Tzetis M, Kanavakis E, Metaxotou-Mavromati A, Kattamis C. Traeger-Synodinos J, et al. Among authors: tzetis m. Br J Haematol. 1991 Oct;79(2):302-5. doi: 10.1111/j.1365-2141.1991.tb04537.x. Br J Haematol. 1991. PMID: 1720325

3

Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.

Metaxotou-Mavromati A, Kattamis C, Matathia L, Tzetis M, Kanavakis E. Metaxotou-Mavromati A, et al. Among authors: tzetis m. J Med Genet. 1988 Mar;25(3):195-9. doi: 10.1136/jmg.25.3.195. J Med Genet. 1988. PMID: 3351907 Free PMC article.

4

Identification of two novel mutations (296 + 1G-C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patients.

Tzetis M, Kanavakis E, Antoniadi T, Traeger-Synodinos J, Doudounakis S, Adam G, Kattamis C. Tzetis M, et al. Mol Cell Probes. 1995 Aug;9(4):283-5. doi: 10.1016/s0890-8508(95)90169-8. Mol Cell Probes. 1995. PMID: 7477025

5

Hematologic phenotype of the mutations IVS1-n6 (T-->C), IVS1-n110 (G-->A), and CD39 (C-->T) in carriers of beta-thalassemia in Greece.

Stefanis L, Kanavakis E, Traeger-Synodinos J, Tzetis M, Metaxotou-Mavromati A, Kattamis C. Stefanis L, et al. Among authors: tzetis m. Pediatr Hematol Oncol. 1994 Sep-Oct;11(5):509-17. doi: 10.3109/08880019409141689. Pediatr Hematol Oncol. 1994. PMID: 7530030

6

Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutation.

Kanavakis E, Tzetis M, Antoniadi T, Traeger-Synodinos J, Doudounakis S, Adam G, Matsaniotis N, Kattamis C. Kanavakis E, et al. Among authors: tzetis m. Hum Genet. 1995 Sep;96(3):364-6. doi: 10.1007/BF00210426. Hum Genet. 1995. PMID: 7544320

7

Molecular characterization of homozygous (high HbA2) beta-thalassemia intermedia in Greece.

Kanavakis E, Traeger-Synodinos J, Tzetis M, Metaxotou-Mavromati A, Ladis V, Kattamis C. Kanavakis E, et al. Among authors: tzetis m. Pediatr Hematol Oncol. 1995 Jan-Feb;12(1):37-45. doi: 10.3109/08880019509029526. Pediatr Hematol Oncol. 1995. PMID: 7703040

8

The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece.

Tzetis M, Traeger-Synodinos J, Kanavakis E, Metaxotou-Mavromati A, Kattamis C. Tzetis M, et al. Hematol Pathol. 1994;8(1-2):25-34. Hematol Pathol. 1994. PMID: 8034555

9

Characterization of nondeletion alpha-thalassemia mutations in the Greek population.

Traeger-Synodinos J, Kanavakis E, Tzetis M, Kattamis A, Kattamis C. Traeger-Synodinos J, et al. Among authors: tzetis m. Am J Hematol. 1993 Nov;44(3):162-7. doi: 10.1002/ajh.2830440305. Am J Hematol. 1993. PMID: 8213764

10

Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations.

Tzetis M, Kanavakis E, Antoniadi T, Doudounakis S, Adam G, Kattamis C. Tzetis M, et al. Hum Genet. 1997 Jan;99(1):121-5. doi: 10.1007/s004390050324. Hum Genet. 1997. PMID: 9003508

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