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Results of search for 'au:"Kanavakis, E"', page 4 of 6
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Authors
Adam, G
Antoniadi, T
Cao, A
Doudounakis, S
Fryssira, H
Kanavakis, E
Kattamis, C
Kitsiou, S
Kitsiou-Tzeli, S
Kolialexi, A
Maragoudaki, E
Mavrou, A
Metaxotou-Mavromati, A
Metaxotou-Mavrommati, A
Papassotiriou, I
Stamoulakatou, A
Traeger-Synodinos, J
Tsezou, A
Tzetis, M
Vrettou, C
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DNA Mutational Analysis
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Mutation
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analysis
blood
diagnosis
genetics
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61.
A new delta chain variant hemoglobin A2-Corfu or alpha 2 delta 2 116 Arg----Cys (G18), detected by delta-globin gene analysis in a Greek family.
[electronic resource]
by
Loudianos, G
Murru, S
Kanavakis, E
Metaxotou-Mavromati, A
Theodoropoulou, D
Kattamis, C
Cao, A
Pirastu, M
Producer:
19910813
In:
Human genetics
vol. 87
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62.
Severe hypertriglyceridaemia in diabetic ketoacidosis: clinical and genetic study.
[electronic resource]
by
Karagianni, C
Stabouli, S
Roumeliotou, K
Traeger-Synodinos, J
Kavazarakis, E
Gourgiotis, D
Lambrou, J
Kanavakis, E
Producer:
20040630
In:
Diabetic medicine : a journal of the British Diabetic Association
vol. 21
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63.
Two-way trafficking of Annexin V positive cells between mother and fetus: determination of apoptosis at delivery.
[electronic resource]
by
Kolialexi, A
Tsangaris, G Th
Anagnostopoulos, A
Chondros, D
Bagiokos, V
Kitsiou, S
Kanavakis, E
Mavrou, A
Producer:
20070605
In:
Prenatal diagnosis
vol. 27
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64.
Association of two DNA polymorphisms in the alpha-globin gene cluster: implications for genetic analysis.
[electronic resource]
by
Wainscoat, J S
Higgs, D R
Kanavakis, E
Cao, A
Georgiou, D
Clegg, J B
Weatherall, D J
Producer:
19840107
In:
American journal of human genetics
vol. 35
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65.
Dysmorphology services: a snapshot of current practices and a vision for the future.
[electronic resource]
by
Douzgou, S
Chervinsky, E
Gyftodimou, Y
Kitsiou-Tzeli, S
Shalev, S
Kanavakis, E
Donnai, D
Clayton-Smith, J
Producer:
20161013
In:
Clinical genetics
vol. 89
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66.
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.
[electronic resource]
by
Kanavakis, E
Tzetis, M
Antoniadi, T
Traeger-Synodinos, J
Doudounakis, S
Adam, G
Matsaniotis, N
Kattamis, C
Producer:
19950928
In:
Human genetics
vol. 96
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67.
The interaction of alpha zero thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H.
[electronic resource]
by
Kanavakis, E
Traeger-Synodinos, J
Papasotiriou, I
Vrettou, C
Metaxotou-Mavromati, A
Stamoulakatou, A
Lagona, E
Kattamis, C
Producer:
19960515
In:
British journal of haematology
vol. 92
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68.
Regional localisation of the human alpha-globin genes.
[electronic resource]
by
Wainscoat, J S
Kanavakis, E
Weatherall, D J
Walker, J
Holmes-Seidle, M
Bobrow, M
Donnison, A B
Producer:
19810925
In:
Lancet (London, England)
vol. 2
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69.
Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience.
[electronic resource]
by
Kanavakis, E
Papassotiriou, I
Karagiorga, M
Vrettou, C
Metaxotou-Mavrommati, A
Stamoulakatou, A
Kattamis, C
Traeger-Synodinos, J
Producer:
20010215
In:
British journal of haematology
vol. 111
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70.
Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations.
[electronic resource]
by
Loudianos, G
Lovicu, M
Solinas, P
Kanavakis, E
Tzetis, M
Manolaki, N
Panagiotakaki, E
Karpathios, T
Cao, A
Producer:
20010329
In:
Genetic testing
vol. 4
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71.
Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probands.
[electronic resource]
by
Traeger-Synodinos, J
Mavroidis, N
Kanavakis, E
Drogari, E
Humphries, S E
Day, I N
Kattamis, C
Matsaniotis, N
Producer:
19980424
In:
Human genetics
vol. 102
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72.
A high incidence of mutations in exon 6 of the low-density lipoprotein receptor gene in Greek familial hypercholesterolemia patients, including a novel mutation.
[electronic resource]
by
Mavroidis, N
Traeger-Synodinos, J
Kanavakis, E
Drogari, E
Matsaniotis, N
Humphries, S E
Day, I N
Kattamis, C
Producer:
19970617
In:
Human mutation
vol. 9
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73.
Steroid hormones polymorphisms and cholelithiasis in Greek population.
[electronic resource]
by
Kitsiou-Tzeli, S
Giannatou, E
Spanos, I
Nicolaidou, P
Fretzayas, A
Tzetis, M
Lazaris, D
Kanavakis, E
Tsezou, A
Producer:
20070417
In:
Liver international : official journal of the International Association for the Study of the Liver
vol. 27
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74.
De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature.
[electronic resource]
by
Kitsiou-Tzeli, Sophia
Tzetis, Maria
Sofocleous, Christalena
Vrettou, Christina
Xaidara, Athena
Giannikou, Krinio
Pampanos, Andreas
Mavrou, Ariadne
Kanavakis, E
Producer:
20101115
In:
American journal of medical genetics. Part A
vol. 152A
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75.
Abnormal mRNA splicing resulting from consensus sequence splicing mutations of ATP7B.
[electronic resource]
by
Loudianos, G
Lovicu, M
Dessi, V
Tzetis, M
Kanavakis, E
Zancan, L
Zelante, L
Galvèz-Galvèz, C
Cao, A
Producer:
20030103
In:
Human mutation
vol. 20
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76.
Association of unstable hemoglobin variants and heterozygous beta-thalassemia: example of a new variant Hb Acharnes or [beta53(D4) Ala --> Thr].
[electronic resource]
by
Papassotiriou, I
Traeger-Synodinos, J
Promé, D
Kister, J
Stamou, E
Liakopoulou, T
Stamoulakatou, A
Kanavakis, E
Wajcman, H
Producer:
19991123
In:
American journal of hematology
vol. 62
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77.
Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis.
[electronic resource]
by
Tzetis, M
Kaliakatsos, M
Fotoulaki, M
Papatheodorou, A
Doudounakis, S
Tsezou, A
Makrythanasis, P
Kanavakis, E
Nousia-Arvanitakis, S
Producer:
20070725
In:
Clinical genetics
vol. 71
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78.
Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.
[electronic resource]
by
Voutoufianakis, S
Psoni, S
Vorgia, P
Tsekoura, F
Kekou, K
Traeger-Synodinos, J
Kitsiou, S
Kanavakis, E
Fryssira, H
Producer:
20070905
In:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
vol. 11
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79.
Cystic fibrosis mutational spectrum and genotypic/phenotypic features in Greek-Cypriots, with emphasis on dehydration as presenting symptom.
[electronic resource]
by
Yiallouros, P K
Neocleous, V
Zeniou, M
Adamidou, T
Costi, C
Christophi, C
Tzetis, M
Kanavakis, E
Deltas, C
Producer:
20070614
In:
Clinical genetics
vol. 71
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80.
Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels.
[electronic resource]
by
Vrettou, C
Kanavakis, E
Traeger-Synodinos, J
Metaxotou-Mavrommati, A
Basiakos, I
Maragoudaki, E
Stamoulakatou, A
Papassotiriou, I
Kattamis, C
Producer:
20010104
In:
Hemoglobin
vol. 24
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