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Search Results - Gyftodimou, Y.
Search Results - Gyftodimou, Y.
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Dysmorphology services: a snapshot of current practices and a vision for the future
by
Douzgou, S.
,
Chervinsky, E.
,
Gyftodimou, Y.
,
Kitsiou-Tzeli, S.
,
Shalev, S.
,
Kanavakis, E.
,
Donnai, D.
,
Clayton-Smith, J.
Published in
Clinical genetics
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Neonatal neuromuscular variant of glycogen storage disease type IV: histopathological findings leading to the diagnosis
by
Konstantinidou, A E
,
Anninos, H
,
Gyftodimou, Y
,
Petersen, M B
,
Karadimas, C
,
Fotopoulos, S
,
Paraskevakou, H
,
Akman, H O
,
DiMauro, S
,
Patsouris, E
Published in
Histopathology
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Osteogenesis imperfecta due to a possible new COL1A2 mutation; the importance of phenotyping and diagnostic challenges
by
Papamerkouriou, Y M
,
Doulgeraki, A
,
Gyftodimou, Y
,
Athanasopoulou, H
,
Tsiridis, E
,
Anastasopoulos, J
Published in
Journal of musculoskeletal & neuronal interactions
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Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16
by
Zollino, Marcella
,
Lecce, Rosetta
,
Murdolo, Marina
,
Orteschi, Daniela
,
Marangi, Giuseppe
,
Selicorni, Angelo
,
Midro, Alina
,
Sorge, Giovanni
,
Zampino, Giuseppe
,
Memo, Luigi
,
Battaglia, Domenica
,
Petersen, Michael
,
Pandelia, Effie
,
Gyftodimou, Yolanda
,
Faravelli, Francesca
,
Tenconi, Romano
,
Garavelli, Livia
,
Mazzanti, Laura
,
Fischetto, Rita
,
Cavalli, Pietro
,
Savasta, Salvatore
,
Rodriguez, Laura
,
Neri, Giovanni
Published in
Human genetics
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Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene dusters nor by inversion polymorphism on 4p16
by
Zollino, M
,
Lecce, R
,
Murdolo, M
,
Orteschi, D
,
Marangi, G
,
Selicorni, A
,
Midro, A
,
Sorge, G
,
Zampino, G
,
Memo, L
,
Battaglia, D
,
Petersen, M
,
Pandelia, E
,
Gyftodimou, Y
Published in
Human genetics
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Neonatal neuromuscular variant of glycogen storage disease type IV: histopathological findings leading to the diagnosis
by
Konstantinidou, A E
,
Anninos, H
,
Gyftodimou, Y
,
Petersen, M B
,
Karadimas, C
,
Fotopoulos, S
,
Paraskevakou, H
,
Akman, H O
,
Dimauro, S
,
Patsouris, E
Published in
Histopathology
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The 11q; 22q translocation: a collaborative study of 20 new cases and analysis of 110 families
by
ISELIUS, L
,
LINDSTEN, J
,
DUTRILLAUX, B
,
FUKUSHIMA, Y
,
GERAETIS, J. P. M
,
DE GROUCHY, J
,
ZUFFARDI, O
,
AURIAS, A
,
FRACCARO, M
,
BASTARD, C
,
BOTTELLI, A. M
,
BUI, T.-H
,
CAUFIN, D
,
DALPRA, L
,
DELENDI, N
Published in
Human genetics
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