Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH von Manolakos, Emmanouil, Kefalas, Konstantinos, Vetro, Annalisa, Oikonomidou, Eirini, Daskalakis, George, Psara, Natasa, Siomou, Elisa, Papageorgiou, Elena, Sevastopoulou, Eirini, Konstantinidou, Anastasia, Vrachnis, Nikolaos, Thomaidis, Loretta, Zuffardi, Orsetta, Papoulidis, Ioannis

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Prenatal diagnosis of Baraitser – Winter syndrome using exome sequencing: Clinical report and review of literature von Papamichail, Maria, Manolakos, Emmanouil, Papoulidis, Ioannis, Siomou, Elisavet, Eleftheriades, Anna, Marinakis, Ioannis, Tzanakis, Konstantinos, Sartsidis, Anastasios, Vlahos, Nikolaos F., Eleftheriades, Makarios

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Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases von Papoulidis, Ioannis, Sotiriadis, Alexandros, Siomou, Elisavet, Papageorgiou, Elena, Eleftheriades, Makarios, Papadopoulos, Vasilios, Oikonomidou, Eirini, Orru, Sandro, Manolakos, Emmanouil, Athanasiadis, Apostolos

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Non‐invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study von Sotiriadis, Alexandros, Papoulidis, Ioannis, Siomou, Elisavet, Papageorgiou, Elena, Eleftheriades, Makarios, Papadopoulos, Vasilios, Alexiou, Maria, Manolakos, Emmanouil, Athanasiadis, Apostolos

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Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search von Vrachnis, Nikolaos, Papoulidis, Ioannis, Vrachnis, Dionysios, Siomou, Elisavet, Antonakopoulos, Nikolaos, Oikonomou, Stavroula, Zygouris, Dimitrios, Loukas, Nikolaos, Iliodromiti, Zoi, Pavlidou, Efterpi, Thomaidis, Loretta, Manolakos, Emmanouil

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Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study: Retrospective study of NIPS versus aCGH von Sotiriadis, Alexandros, Papoulidis, Ioannis, Siomou, Elisavet, Papageorgiou, Elena, Eleftheriades, Makarios, Papadopoulos, Vasilios, Alexiou, Maria, Manolakos, Emmanouil, Athanasiadis, Apostolos

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Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases:... von Papoulidis, Ioannis, Sotiriadis, Alexandros, Siomou, Elisavet, Papageorgiou, Elena, Eleftheriades, Makarios, Papadopoulos, Vasilios, Oikonomidou, Eirini, Orru, Sandro, Manolakos, Emmanouil, Athanasiadis, Apostolos

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Vitamin D status and cardiometabolic risk factors in Greek adolescents with obesity - the effect of vitamin D supplementation: a pilot study von Makariou, Stefania E, Challa, Anna, Siomou, Ekaterini, Tellis, Constantinos, Tselepis, Alexandros, Elisaf, Moses, Liberopoulos, Evangelos

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Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report von Orru, Sandro, Papoulidis, Ioannis, Siomou, Elisavet, Papadimitriou, Dimitrios T, Sotiriou, Sotirios, Nikolaidis, Petros, Eleftheriades, Makarios, Papanikolaou, Evaggelos, Thomaidis, Loretta, Manolakos, Emmanouil

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Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13 500 cases with consideration of using QF-PCR as a stand-alone... von Papoulidis, Ioannis, Siomou, Elisavet, Sotiriadis, Alexandros, Efstathiou, George, Psara, Anastasia, Sevastopoulou, Eirini, Anastasakis, Eleftherios, Sifakis, Stavros, Tsiligianni, Theodora, Kontodiou, Maria, Malamaki, Christine, Tzimina, Maria, Petersen, Michael Bjorn, Manolakos, Emmanouil, Athanasiadis, Apostolos

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Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities von Dagklis, Themistoklis, Papageorgiou, Elena, Siomou, Elisavet, Paspaliaris, Vassilis, Zerva, Christina, Chatzis, Panagiotis, Thomaidis, Loretta, Manolakos, Emmanouil, Papoulidis, Ioannis

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A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2 von Siomou, Elisavet, Manolakos, Emmanouil, Petersen, Michael, Thomaidis, Loretta, Gyftodimou, Yolanda, Orru, Sandro, Papoulidis, Ioannis

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Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334-kb deletion: A case report von PAPOULIDIS, IOANNIS, OIKONOMIDOU, EIRINI, ORRU, SANDRO, SIOMOU, ELISAVET, KONTODIOU, MARIA, ELEFTHERIADES, MAKARIOS, BACOULAS, VASILIOS, CIGUDOSA, JUAN C, SUELA, JAVIER, THOMAIDIS, LORETTA, MANOLAKOS, EMMANOUIL

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Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization von Kontodiou, Maria, Paspaliaris, Vassilis, Dagklis, Themistoklis, Siomou, Elisavet, Hamid Al-Rikabi, Ahmed, Tsita, Kalliopi, Stavroulaki, Theano, Pampanos, Andreas, Zavlanos, Apostolos, Papaioannou, Georgios, Papoulidis, Ioannis, Thomaidis, Loretta, Manolakos, Emmanouil

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Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male von Papoulidis, Ioannis, Paspaliaris, Vassilis, Siomou, Elisavet, Orru, Sandro, Murru, Roberta, Sifakis, Stavros, Nikolaidis, Petros, Garas, Antonios, Sotiriou, Sotirios, Thomaidis, Loretta, Manolakos, Emmanouil

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A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth von Papoulidis, Ioannis, Manolakos, Emmanouil, Siomou, Elisavet, Kefalas, Kostantinos, Thomaidis, Loretta, Liehr, Thomas, Vetro, Annalisa, Athanasiadis, Apostolos, Zuffardi, Orsetta, Petersen, Michael B.

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Children with metabolically healthy obesity have a worse metabolic profile compared to normal-weight peers: a cross-sectional study von Serbis, Anastasios, Giapros, Vasilieios, Paschou, Stavroula A., Siomou, Ekaterini

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Elevated 1‐hour post‐load plasma glucose identifies obese youth with abnormal glucose metabolism and an unfavourable inflammatory profile von Serbis, Anastasios, Giapros, Vasileios, Challa, Anna, Chaliasos, Nikolaos, Siomou, Ekaterini

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Intact FGF23 and Markers of Iron Homeostasis, Inflammation, and Bone Mineral Metabolism in Acute Pediatric Infections von Papastergiou, Eleni, Rallis, Dimitrios, Papagianni, Afroditi, Cholevas, Vasileios, Katzilakis, Nikolaos, Siomou, Ekaterini, Stiakaki, Eftichia, Makis, Alexandros

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Persistent mild hypokalemia in an otherwise healthy 6-year-old girl: Answers von Roumeliotou, Sofia, Theohari, Anastasia, Tsamoulis, Donatos, Vafeidou, Kyriaki, Siountri, Iliana, Siomou, Ekaterini

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