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Author
8
Georgiou, I.
4
Grigoriadou, M.
4
Petersen, M. B.
3
Bouba, I.
3
Chatzikyriakidou, A.
3
Eleftheriades, N.
3
Elisaf, M. S.
3
Iliades, T.
3
Iliadou, V.
3
Pampanos, A.
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Humans
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*Mutation
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Adult
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Greece/epidemiology
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Genetic Testing
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Adolescent
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22
journalArticle
Date
2
2010 - 2011
19
2000 - 2009
1
1991 - 1999
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ΑΠΟΘΕΤΗΡΙΟ "ΟΛΥΜΠΙΑΣ"
Σχολή Επιστημών Υγείας
Τμήμα Ιατρικής
Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Role of proline residues in the structure and function of a membrane transport protein (Journal article)
Detection and mutation screening of Malassezia sympodialis sequences coding for the Mal s 1 allergen implicated in atopic dermatitis (Journal article)
Lack of association between the C677T mutation in the 5,10-methylenetetrahydrofolate reductase gene and venous thromboembolism in Northwestern Greece (Journal article)
Prevalence of GJB2 mutations in prelingual deafness in the Greek population (Journal article)
Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings (Journal article)
Delta-thalassemia in Cyprus (Journal article)
Spectrum of LDLR gene mutations, including a novel mutation causing familial hypercholesterolaemia, in North-western Greece (Journal article)
Non-invasive first-trimester detection of paternal beta-globin gene mutations and polymorphisms as predictors of thalassemia risk at chorionic villous sampling (Journal article)
Novel human pathological mutations. Gene symbol: SLC3A1. Disease: Cystinuria (Journal article)
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia (Journal article)