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Repository of UOI "Olympias"
Repository of OAI
Browsing by Author Papoulidis, I.
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Showing results 1 to 5 of 5
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Author(s)
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Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization
Manolakos, E.
;
Kefalas, K.
;
Neroutsou, R.
;
Lagou, M.
;
Kosyakova, N.
;
Ewers, E.
;
Ziegler, M.
;
Weise, A.
;
Tsoplou, P.
;
Rapti, S. M.
;
Papoulidis, I.
;
Anastasakis, E.
;
Garas, A.
;
Sotiriou, S.
;
Eleftheriades, M.
;
Peitsidis, P.
;
Malathrakis, D.
;
Thomaidis, L.
;
Kitsos, G.
;
Orru, S.
;
Liehr, T.
;
Petersen, M. B.
;
Kitsiou-Tzeli, S.
24-Nov-2015
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Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation
Manolakos, E.
;
Vetro, A.
;
Kefalas, K.
;
Thomaidis, L.
;
Aperis, G.
;
Sotiriou, S.
;
Kitsos, G.
;
Merkas, M.
;
Sifakis, S.
;
Papoulidis, I.
;
Liehr, T.
;
Zuffardi, O.
;
Petersen, M. B.
24-Nov-2015
-
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)
Manolakos, E.
;
Orru, S.
;
Neroutsou, R.
;
Kefalas, K.
;
Louizou, E.
;
Papoulidis, I.
;
Thomaidis, L.
;
Peitsidis, P.
;
Sotiriou, S.
;
Kitsos, G.
;
Tsoplou, P.
;
Petersen, M. B.
;
Metaxotou, A.
24-Nov-2015
-
A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth
Papoulidis, I.
;
Manolakos, E.
;
Siomou, E.
;
Kefalas, K.
;
Thomaidis, L.
;
Liehr, T.
;
Vetro, A.
;
Athanasiadis, A.
;
Zuffardi, O.
;
Petersen, M. B.
24-Nov-2015
-
Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature
Manolakos, E.
;
Sifakis, S.
;
Sotiriou, S.
;
Peitsidis, P.
;
Eleftheriades, M.
;
Mersinias, V.
;
Liehr, T.
;
Thomaidis, L.
;
Kitsos, G.
;
Papoulidis, I.
;
Petersen, M. B.
;
Orru, S.
24-Nov-2015
-