ΠΡΟΣΩΠΟ – Βιβλιοnet
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases - Papoulidis - 2015 - Prenatal Diagnosis - Wiley Online Library
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
Loop | IOANNIS PAPOULIDIS
Molecular Cytogenetics Research Papers - Academia.edu
Ioannis Papoulidis - Senior Funds Accountant - Alter Domus | LinkedIn
Ιωάννης Βαρβάκης - Βικιπαίδεια
Ευεργέτες δύο πατρίδων, Ιωάννης Βαρβάκης (1750-1824), Δημήτριος Μπερναδράκης (1799-1870), Γρηγόριος Μαρασλής (1831-1907) - Κωνσταντίνος Κ. Παπουλίδης | Skroutz.gr
PDF) Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report | Makarios Eleftheriades - Academia.edu
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
Συμβουλευτική στο ελεύθερο εμβρυικό DNA: «Λοιπά γενετικά σύνδρομα» – Ελληνική Εταιρία Εμβρυομητρικής Ιατρικής
Best Practices in PGT 2019 – Embryolab Academy
A novel familial mutation associated with Treacher Collins syndrome: A case report
Γιάννης Παπουλίδης Archives - Ο Ντελάλης
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Medicina | Free Full-Text | A New ABCA3 Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome
Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search | Molecular Cytogenetics | Full Text
Loop | Georgios S Markopoulos
Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο
