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Personnel - ATG Genetics Laboratories

Personnel - ATG Genetics Laboratories

Medicina | October 2022 - Browse Articles

Medicina | October 2022 - Browse Articles

Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki | Research profile

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Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki | Research profile

Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki | Research profile

Σταμάτης Παπουλίδης | Τεχνικό Γραφείο - Μηχανολόγος Μηχανικός | Έκδοση Αδειών Κυκλοφορίας Μηχανημάτων Έργων | Μηχανολογικές Mελέτες | Μεταβιβάσεις | Διαγραφές | Ακινητοποιήσεις κ.α.

Σταμάτης Παπουλίδης | Τεχνικό Γραφείο - Μηχανολόγος Μηχανικός | Έκδοση Αδειών Κυκλοφορίας Μηχανημάτων Έργων | Μηχανολογικές Mελέτες | Μεταβιβάσεις | Διαγραφές | Ακινητοποιήσεις κ.α.

Ioannis Papoulidis | LinkedIn

Ioannis Papoulidis | LinkedIn

Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο

2017-09-27 10:47

2017-09-27 10:47

Ioannis Papoulidis | LinkedIn

ioannis pappas - Greece | Professional Profile | LinkedIn

Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki | Research profile

PDF) Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization

PDF) Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization

Ioannis Papoulidis | LinkedIn

Ioannis Papoulidis | LinkedIn

Ioannis Papoulidis | LinkedIn

Ioannis Papoulidis | LinkedIn

Ioannis Papoulidis | LinkedIn

Ioannis Papoulidis | LinkedIn

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library

PDF) Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies

PDF) Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies

Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki | Research profile

PDF) Routine use of Array Comparative Genomic Hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1,763 prenatal cases

PDF) Routine use of Array Comparative Genomic Hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1,763 prenatal cases

ΒΛΑΧΟΣ ΙΩΑΝΝΗΣ Η. Ορθοπεδικός | Μαρούσι Αττικής | 2106867774 | xo.gr

ΒΛΑΧΟΣ ΙΩΑΝΝΗΣ Η. Ορθοπεδικός | Μαρούσι Αττικής | 2106867774 | xo.gr

Έρευνα - Εργασίες - Ιωάννης Α. Παναγιωτόπουλος

Έρευνα - Εργασίες - Ιωάννης Α. Παναγιωτόπουλος

Children | Special Issue : Developmental and Behavioral Pediatrics

Children | Special Issue : Developmental and Behavioral Pediatrics

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library

PDF) A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth | Ioannis Papoulidis, O. Zuffardi, A. Athanasiadis, Elisavet Siomou, and Emanouil Manolakos - Academia.edu

PDF) A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth | Ioannis Papoulidis, O. Zuffardi, A. Athanasiadis, Elisavet Siomou, and Emanouil Manolakos - Academia.edu

PDF) Linkage analysis in bipolar pedigrees adds support for a susceptibility locus on 21q22

PDF) Linkage analysis in bipolar pedigrees adds support for a susceptibility locus on 21q22