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Results of search for 'au:"Kanavakis, E"', page 3 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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Adolescent
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Child, Preschool
DNA Mutational Analysis
Female
Genotype
Globins
Greece
Heterozygote
Humans
Infant
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Mutation
Phenotype
Thalassemia
analysis
blood
diagnosis
genetics
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Serbian
Your search returned 101 results.
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41.
MicroRNA expression profiles in pediatric dysembryoplastic neuroepithelial tumors.
[electronic resource]
by
Braoudaki, M
Lambrou, G I
Papadodima, S A
Stefanaki, K
Prodromou, N
Kanavakis, E
Producer:
20160907
In:
Medical oncology (Northwood, London, England)
vol. 33
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42.
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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43.
Globin gene mapping in normal Hb A2 types of beta-thalassaemia.
[electronic resource]
by
Kanavakis, E
Metaxotou-Mavromati, A
Kattamis, C
Aksoy, M
Weatherall, D J
Wood, W G
Producer:
19820722
In:
British journal of haematology
vol. 51
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44.
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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45.
Long term follow up of a woman with classic form of Ehlers-Danlos syndrome associated with rare manifestations and review of the literature.
[electronic resource]
by
Kitsiou-Tzeli, S
Leze, E
Salavoura, K
Giannatou, E
Fretzayas, A
Makrithanasis, P
Kanavakis, E
Producer:
20100514
In:
Genetic counseling (Geneva, Switzerland)
vol. 21
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46.
Unilateral microtia in an infant with trisomy 18 mosaicism.
[electronic resource]
by
Giannatou, E
Leze, H
Katana, A
Kolialexi, A
Mavrou, A
Kanavakis, E
Kitsiou-Tzeli, S
Producer:
20090928
In:
Genetic counseling (Geneva, Switzerland)
vol. 20
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47.
Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemia.
[electronic resource]
by
Traeger-Synodinos, J
Harteveld, C L
Kanavakis, E
Giordano, P C
Kattamis, C
Bernini, L F
Producer:
19991223
In:
Hemoglobin
vol. 23
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48.
Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha2, codon 59, GGC-->GAC) or a nondeletional alpha-thalassemia mutation (AATAAA-->AATAAG): comparison of phenotypes illustrating "dominant" alpha-thalassemia.
[electronic resource]
by
Traeger-Synodinos, J
Metaxotou-Mavrommati, A
Karagiorga, M
Vrettou, C
Papassotiriou, I
Stamoulakatou, A
Kanavakis, E
Producer:
19991223
In:
Hemoglobin
vol. 23
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49.
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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50.
Severe Developmental Delay in a Patient with 7p21.1-p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene Cluster.
[electronic resource]
by
Fryssira, H
Makrythanasis, P
Kattamis, A
Stokidis, K
Menten, B
Kosaki, K
Willems, P
Kanavakis, E
Publication details:
Molecular syndromology
Dec 2011
In:
Molecular syndromology
vol. 2
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51.
CFTR gene mutations--including three novel nucleotide substitutions--and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease.
[electronic resource]
by
Tzetis, M
Efthymiadou, A
Strofalis, S
Psychou, P
Dimakou, A
Pouliou, E
Doudounakis, S
Kanavakis, E
Producer:
20010531
In:
Human genetics
vol. 108
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52.
Association of repeat polymorphisms in the estrogen receptors alpha, beta (ESR1, ESR2) and androgen receptor (AR) genes with the occurrence of breast cancer.
[electronic resource]
by
Tsezou, A
Tzetis, M
Gennatas, C
Giannatou, E
Pampanos, A
Malamis, G
Kanavakis, E
Kitsiou, S
Producer:
20080717
In:
Breast (Edinburgh, Scotland)
vol. 17
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53.
An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant.
[electronic resource]
by
Traeger-Synodinos, J
Metaxotou-Mavromati, A
Kanavakis, E
Vrettou, C
Papassotiriou, I
Michael, T
Kattamis, C
Producer:
19980908
In:
Hemoglobin
vol. 22
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54.
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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55.
Mutation spectrum and phenotypic manifestation in FSHD Greek patients.
[electronic resource]
by
Sakellariou, P
Kekou, K
Fryssira, H
Sofocleous, C
Manta, P
Panousopoulou, A
Gounaris, K
Kanavakis, E
Producer:
20120801
In:
Neuromuscular disorders : NMD
vol. 22
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56.
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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57.
Noninvasive prenatal diagnosis of beta-thalassaemia using individual fetal erythroblasts isolated from maternal blood after enrichment.
[electronic resource]
by
Kolialexi, A
Vrettou, C
Traeger-Synodinos, J
Burgemeister, R
Papantoniou, N
Kanavakis, E
Antsaklis, A
Mavrou, A
Producer:
20080325
In:
Prenatal diagnosis
vol. 27
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58.
Pregnancies following blastocyst stage transfer in PGD cycles at risk for beta-thalassaemic haemoglobinopathies.
[electronic resource]
by
Palmer, G A
Traeger-Synodinos, J
Davies, S
Tzetis, M
Vrettou, C
Mastrominas, M
Kanavakis, E
Producer:
20020326
In:
Human reproduction (Oxford, England)
vol. 17
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59.
Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes.
[electronic resource]
by
Maragoudaki, E
Kanavakis, E
Traeger-Synodinos, J
Vrettou, C
Tzetis, M
Metaxotou-Mavrommati, A
Kattamis, C
Producer:
20000210
In:
British journal of haematology
vol. 107
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60.
The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.
[electronic resource]
by
Traeger-Synodinos, J
Kanavakis, E
Vrettou, C
Maragoudaki, E
Michael, T
Metaxotou-Mavromati, A
Kattamis, C
Producer:
19970117
In:
British journal of haematology
vol. 95
Online resources:
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