NKX2.5 as a modifier gene of the cardiac phenotype in patients with the 22q11 deletion syndrome (Bachelor thesis)

Papaioannou, Maria-Eleni

Institution and School/Department of submitter: Δημοκρίτειο Πανεπιστήμιο Θράκης/Σχολή Επιστημών Υγείας/Τμήμα Μοριακής Βιολογίας και Γενετικής
Subject classification: Modifiers (genes)
Deletion syndrome
Keywords: Deletion syndrome,Modifier gene,Cardiac phenotype
URI: https://repo.lib.duth.gr/jspui/handle/123456789/6099
http://dx.doi.org/10.26257/heal.duth.6485
Appears in Collections:ΤΜΗΜΑ ΜΟΡΙΑΚΗΣ ΒΙΟΛΟΓΙΑΣ & ΓΕΝΕΤΙΚΗΣ

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https://repo.lib.duth.gr/jspui/handle/123456789/6099
http://dx.doi.org/10.26257/heal.duth.6485
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