Diagnosis of Fanconi Anaemia (FA) in dizygotic twins

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Diagnosis of Fanconi Anaemia (FA) in dizygotic twins

Please use any of these identifiers to cite or link to this item:
http://hdl.handle.net/10795/3636
http://repository.edulll.gr/3636

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Abstract	In this study we report on a case of FA in dizygotic twins with characteristic congenital abnormalities and the same deletions of the FANCA gene.
Author/Creator	Selenti, N.; Kolialexi, A.; Papadakis, V.; Avgerinou, G.; Roka, K.; Polychronopoulou, S.; Kanavakis, E.; Mavrou, A.
Contractor	Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)
Language	English
Date	2011
Extent	1 pages
Subject	υγεία φυσικές επιστήμες κυτταρολογία
Keywords	Fanconi anemia, FANCA gene, Genetic disorders, Genes, DNA, Dizygotic twins, Κύτταρα, Γονίδια, Γενετικές διαταραχές, Διζυγωτικά δίδυμα
Is Related to	Investigation of FANCA mutations in greek patients Cytogenetic and molecular investigation of greek patients referred for Fanconi Anaemia
Type	Text (Conference or workshop item (Poster))
Scientific Coordinator	Μαύρου-Καλπίνη, Αριάδνη
Project Notes	Πράξη: Κυτταρογενετικη και Μοριακή Διερεύνηση της Αναιμίας Fanconi Δράση: Ηράκλειτος II