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Results of search for 'au:"Tzetis, M"', page 1 of 3
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Authors
Adam, G
Antoniadi, T
Bombieri, C
Cao, A
Claustres, M
Cuppens, H
Cutting, G R
Doudounakis, S
Efthymiadou, A
Kanavakis, E
Karpathios, T
Kattamis, C
Kitsiou-Tzeli, S
Maragoudaki, E
Mastrominas, M
Metaxotou-Mavromati, A
Traeger-Synodinos, J
Tsezou, A
Tzetis, M
Vrettou, C
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Topics
Adolescent
Adult
Alleles
Child
Child, Preschool
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
DNA Mutational Analysis
Female
Genotype
Globins
Greece
Heterozygote
Humans
Male
Mutation
Phenotype
beta-Thalassemia
diagnosis
genetics
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English
Your search returned 41 results.
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Results
1.
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 gene.
[electronic resource]
by
Tzetis, M
Efthymiadou, A
Doudounakis, S
Kanavakis, E
Producer:
20020215
In:
Human genetics
vol. 109
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2.
Anton van Leeuwenhoek (1632-1723): father of micromorphology and discoverer of spermatozoa.
[electronic resource]
by
Karamanou, M
Poulakou-Rebelakou, E
Tzetis, M
Androutsos, G
Producer:
20110315
In:
Revista Argentina de microbiologia
vol. 42
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3.
Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.
[electronic resource]
by
Metaxotou-Mavromati, A
Kattamis, C
Matathia, L
Tzetis, M
Kanavakis, E
Producer:
19880510
In:
Journal of medical genetics
vol. 25
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4.
Characterization of nondeletion alpha-thalassemia mutations in the Greek population.
[electronic resource]
by
Traeger-Synodinos, J
Kanavakis, E
Tzetis, M
Kattamis, A
Kattamis, C
Producer:
19931119
In:
American journal of hematology
vol. 44
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5.
Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations.
[electronic resource]
by
Tzetis, M
Kanavakis, E
Antoniadi, T
Doudounakis, S
Adam, G
Kattamis, C
Producer:
19970220
In:
Human genetics
vol. 99
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6.
Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia.
[electronic resource]
by
Kanavakis, E
Tzetis, M
Antoniadi, T
Pistofidis, G
Milligos, S
Kattamis, C
Producer:
19990104
In:
Molecular human reproduction
vol. 4
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7.
A Caucasian boy with Gilbert's syndrome heterozygous for the (TA)(8) allele.
[electronic resource]
by
Tsezou, A
Tzetis, M
Kitsiou, S
Kavazarakis, E
Galla, A
Kanavakis, E
Producer:
20000816
In:
Haematologica
vol. 85
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8.
The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalence.
[electronic resource]
by
Traeger-Synodinos, J
Tzetis, M
Kanavakis, E
Metaxotou-Mavromati, A
Kattamis, C
Producer:
19920107
In:
British journal of haematology
vol. 79
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9.
The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece.
[electronic resource]
by
Tzetis, M
Traeger-Synodinos, J
Kanavakis, E
Metaxotou-Mavromati, A
Kattamis, C
Producer:
19940815
In:
Hematologic pathology
vol. 8
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10.
Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individuals.
[electronic resource]
by
Kanavakis, E
Efthymiadou, A
Strofalis, S
Doudounakis, S
Traeger-Synodinos, J
Tzetis, M
Producer:
20031224
In:
Clinical genetics
vol. 63
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11.
Preimplantation genetic diagnosis in 10 couples at risk for transmitting beta-thalassaemia major: clinical experience including the initiation of six singleton pregnancies.
[electronic resource]
by
Kanavakis, E
Vrettou, C
Palmer, G
Tzetis, M
Mastrominas, M
Traeger-Synodinos, J
Producer:
20000228
In:
Prenatal diagnosis
vol. 19
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12.
Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methods.
[electronic resource]
by
Kanavakis, E
Traeger-Synodinos, J
Vrettou, C
Maragoudaki, E
Tzetis, M
Kattamis, C
Producer:
19970924
In:
Molecular human reproduction
vol. 3
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13.
Hematologic phenotype of the mutations IVS1-n6 (T-->C), IVS1-n110 (G-->A), and CD39 (C-->T) in carriers of beta-thalassemia in Greece.
[electronic resource]
by
Stefanis, L
Kanavakis, E
Traeger-Synodinos, J
Tzetis, M
Metaxotou-Mavromati, A
Kattamis, C
Producer:
19950221
In:
Pediatric hematology and oncology
vol. 11
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14.
Molecular characterization of homozygous (high HbA2) beta-thalassemia intermedia in Greece.
[electronic resource]
by
Kanavakis, E
Traeger-Synodinos, J
Tzetis, M
Metaxotou-Mavromati, A
Ladis, V
Kattamis, C
Producer:
19950510
In:
Pediatric hematology and oncology
vol. 12
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15.
Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population.
[electronic resource]
by
Kavazarakis, E
Tsezou, A
Tzetis, M
Hadjidimoula, A
Kitsiou, S
Kanavakis, E
Karpathios, T
Producer:
20010531
In:
European journal of pediatrics
vol. 159
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16.
Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation.
[electronic resource]
by
Kanavakis, E
Tzetis, M
Antoniadi, T
Trager-Synodinos, J
Kattamis, C
Doudounakis, S
Adam, G
Producer:
19950823
In:
Journal of medical genetics
vol. 32
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17.
Identification of two novel mutations (296 + 1G-C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patients.
[electronic resource]
by
Tzetis, M
Kanavakis, E
Antoniadi, T
Traeger-Synodinos, J
Doudounakis, S
Adam, G
Kattamis, C
Producer:
19951218
In:
Molecular and cellular probes
vol. 9
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18.
A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosis.
[electronic resource]
by
Vrettou, C
Palmer, G
Kanavakis, E
Tzetis, M
Antoniadi, T
Mastrominas, M
Traeger-Synodinos, J
Producer:
20000228
In:
Prenatal diagnosis
vol. 19
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19.
Asporin and knee osteoarthritis in patients of Greek origin.
[electronic resource]
by
Kaliakatsos, M
Tzetis, M
Kanavakis, E
Fytili, P
Chouliaras, G
Karachalios, Th
Malizos, K
Tsezou, A
Producer:
20061109
In:
Osteoarthritis and cartilage
vol. 14
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20.
Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.
[electronic resource]
by
Christopoulou, G
Tzetis, M
Konstantinidou, A E
Tsezou, A
Kanavakis, E
Kitsiou-Tzeli, S
Velissariou, V
Producer:
20120605
In:
European journal of medical genetics
vol. 55
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