Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II von Lamb, Neil E, Freeman, Sallie B, Savage-Austin, Amanda, Pettay, Dorothy, Taft, Lisa, Hersey, Jane, Gu, Yuanchao, Shen, Joe, Saker, Denise, May, Kristen M, Avramopoulos, Dimitris, Petersen, Michael B, Hallberg, Anni, Mikkelsen, Margareta, Hassold, Terry J, Sherman, Stephanie L

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Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism von Karadima, G, Bugge, M, Nicolaidis, P, Vassilopoulos, D, Avramopoulos, D, Grigoriadou, M, Albrecht, B, Passarge, E, Annerén, G, Blennow, E, Clausen, N, Galla-Voumvouraki, A, Tsezou, A, Kitsiou-Tzeli, S, Hahnemann, J M, Hertz, J M, Houge, G, Kuklík, M, Macek, M, Lacombe, D, Miller, K, Moncla, A, López Pajares, I, Patsalis, P C, Petersen, M B

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Europe at a Crossroads: Responding to the Global Challenges of Migration and Security von Avramopoulos, Dimitris

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Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations von PANAS, MARIOS, KARADIMAS, CHARALAMBOS, AVRAMOPOULOS, DIMITRIS, VASSILOPOULOS, DEMETRIS

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Characterization of Susceptible Chiasma Configurations that Increase the Risk for Maternal Nondisjunction of Chromosome 21 von Lamb, Neil E., Feingold, Eleanor, Savage, Amanda, Avramopoulos, Dimitris, Freeman, Sallie, Gu, Yuanchao, Hallberg, Anni, Hersey, Jane, Karadima, Georgia, Pettay, Dorothy, Saker, Denise, Shen, Joe, Taft, Lisa, Mikkelsen, Margareta, Petersen, Michael B., Hassold, Terry, Sherman, Stephanie L.

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Elucidating the Mechanisms of Paternal Non-Disjunction of Chromosome 21 in Humans von Savage, Amanda R., Petersen, Michael B., Pettay, Dorothy, Taft, Lisa, Allran, Katherine, Freeman, Sallie B., Karadima, Georgia, Avramopoulos, Dimitris, Torfs, Claudine, Mikkelsen, Margareta, Hassold, Terry J., Sherman, Stephanie L.

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Apolipoprotein E allele distribution in parents of Down's syndrome children von Avramopoulos, D., Grigoriadou, M., Petersen, M.B., Mikkelsen, M., Petersen, M.B., Vassilopoulos, D.

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Apolipoprotein E polymorphism in the Greek population von Sklavounou, Ekaterini, Economou-Petersen, Effrosini, Karadima, Georgia, Panas, Marios, Avramopoulos, Dimitris, Varsou, Angeliki, Vassilopoulos, Dimitris, Petersen, Michael B.

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A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region von BARTSCH, O, HINKEL, G. K, PETERSEN, M. B, KÖNIG, U, BUGGE, M, MIKKELSEN, M, AVRAMOPOULOS, D, MORRIS, M, ANTONARAKIS, S. E

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Exclusion of one pedigree affected by adult onset primary open angle glaucoma from linkage to the juvenile glaucoma locus on chromosome 1q21-q31 von Avramopoulos, D, Kitsos, G, Economou-Petersen, E, Grigoriadou, M, Vassilopoulos, D, Papageorgiou, C, Psilas, K, Petersen, M B

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Polymorphic dinucleotide repeats at the D3S1417, D3S1418 and D12S271 loci von Talbot, C. Conover, Warren, Andrew C., Avramopoulos, Dimitris, Antonarakis, Stylianos E.

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Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome von Petersen, Michael B., Karadima, Georgia, Samaritaki, Maria, Avramopoulos, Dimitris, Vassilopoulos, Dimitris, Mikkelsen, Margareta

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Έκθεση της Διαρκούς Επιτροπής Οικονομικών Υποθέσεων στο σχέδιο νόμου του Υπουργείου Οικονομίας και Οικονομικών "Σύσταση Εθνικού Ταμείου Κοινωνικής συνοχής και άλλες διατάξεις"... von Αλογοσκούφης, Γεώργιος, Φώλιας, Χρήστος, Μαγγίνας, Βασίλης, Παυλόπουλος, Προκόπης, Σπηλιωτόπουλος, Άρης, Αβραμόπουλος, Δημήτρης, Pavlopoulos, Prokopis, Folias, Christos, Alogoskoufis, Georgios, Spiliotopoulos, Aris, Magginas, Vasilis, Avramopoulos, Dimitris

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Θεσμικό πλαίσιο για τις μεταπτυχιακές σπουδές von Αλογοσκούφης, Γεώργιος, Πάλλη-Πετραλιά, Φάνη, Φώλιας, Χρήστος, Στυλιανίδης, Ευριπίδης, Τασούλας, Κωνσταντίνος, Παυλόπουλος, Προκόπης, Αβραμόπουλος, Δημήτρης, Pavlopoulos, Prokopis, Folias, Christos, Alogoskoufis, Georgios, Tasoulas, Konstantinos, Palli-Petralia, Fani, Avramopoulos, Dimitris, Stylianidis, Eyripidis

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Εταιρική κοινωνική ευθύνη von χ.ο, s.n

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On the QKD Integration in Converged Fiber/Wireless Topologies for Secured, Low-Latency 5G/B5G Fronthaul von Zavitsanos, Dimitris, Ntanos, Argiris, Giannoulis, Giannis, Avramopoulos, Hercules

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Studies on the readability and on the detection rate in a Mach–Zehnder interferometer-based implementation for high-rate, long-distance QKD protocols von Papapanos, Christos, Zavitsanos, Dimitris, Raptakis, Adam, Giannoulis, Giannis, Kouloumentas, Christos, Avramopoulos, Hercules

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Feasibility Analysis of QKD Integration in Real-World FTTH Access Networks von Zavitsanos, Dimitris, Ntanos, Argiris, Stathopoulos, Theofanis, Raptakis, Adam, Setaki, Fotini, Lyberopoulos, George, Kouloumentas, Christos, Giannoulis, Giannis, Avramopoulos, Hercules

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Novel Benes Network Routing Algorithm and Hardware Implementation von Nikolaidis, Dimitris, Groumas, Panos, Kouloumentas, Christos, Avramopoulos, Hercules

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Exome sequencing in 53 sporadic cases of schizophrenia identifies 18 putative candidate genes von Guipponi, Michel, Santoni, Federico A, Setola, Vincent, Gehrig, Corinne, Rotharmel, Maud, Cuenca, Macarena, Guillin, Olivier, Dikeos, Dimitris, Georgantopoulos, Georgios, Papadimitriou, George, Curtis, Logos, Méary, Alexandre, Schürhoff, Franck, Jamain, Stéphane, Avramopoulos, Dimitri, Leboyer, Marion, Rujescu, Dan, Pulver, Ann, Campion, Dominique, Siderovski, David P, Antonarakis, Stylianos E

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