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Repository of UOI "Olympias"
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Author
3
Syrrou, M.
2
Bourantas, K. L.
2
Chatzikyriakidou, A.
2
Pagoulatos, G.
2
Patsalis, P. C.
2
Seferiadis, K.
1
Anastasiadou, V.
1
Bondis, I. N.
1
Bouba, I.
1
Boumba, I.
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Humans
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Greece/epidemiology
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Child, Preschool
3
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Cyprus/epidemiology
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*Mutation
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*Nuclear Proteins
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*Point Mutation
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7
journalArticle
Date
3
2000 - 2009
4
1994 - 1999
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ΑΠΟΘΕΤΗΡΙΟ "ΟΛΥΜΠΙΑΣ"
ΨΗΦΙΑΚΗ ΒΙΒΛΙΟΘΗΚΗ "Ηπειρομνήμων"
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Results 1-7 of 7 (Search time: 0.004 seconds).
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R831X mutation of the androgen receptor gene in an adolescent with complete androgen insensitivity syndrome and bilateral testicular hamartomata (Journal article)
Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability (Journal article)
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population (Journal article)
Gamma-chain heterogeneity in Greek (delta beta)zero-thalassemia (Journal article)
Fetal globin stimulation during a short-term trial of erythropoietin in HbS/beta-thalassemia patients (Journal article)
Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations (Journal article)
Absence of mutations of the EPO-receptor gene in Greek patients with familial polycythemia (Journal article)