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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 | Molecular Cytogenetics | Full Text
OLD FOOTBALL - Εμφάνιση άρθρων βάσει ετικέτας: Παπουλίδης Γιάννης
Ιωάννης Βαρβάκης - Βικιπαίδεια
Medicina | Free Full-Text | A New ABCA3 Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome
Speakers-2019 – Abilities Days
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) – topic of research paper in Clinical medicine. Download scholarly article PDF and read for
Συμβουλευτική στο ελεύθερο εμβρυικό DNA: «Λοιπά γενετικά σύνδρομα» – Ελληνική Εταιρία Εμβρυομητρικής Ιατρικής
ΠΡΟΣΩΠΟ – Βιβλιοnet
Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Loop | Georgios S Markopoulos
Best Practices in PGT 2019 – Embryolab Academy
Loop | IOANNIS PAPOULIDIS
Ευεργέτες δύο πατρίδων, Ιωάννης Βαρβάκης (1750-1824), Δημήτριος Μπερναδράκης (1799-1870), Γρηγόριος Μαρασλής (1831-1907) - Κωνσταντίνος Κ. Παπουλίδης | Skroutz.gr
Γιάννης Παπουλίδης Archives - Ο Ντελάλης
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
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
ΔΗΜΟΣΙΕΥΣΕΙΣ - ATG Πρότυπο Διαγνωστικό Κέντρο
Ο Διευθυντής του εργαστηρίου... - ATG - Access To Genome | Facebook
Speakers-2019 – Abilities Days
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
Γιάννης Παπουλίδης (@JonAPap) / Twitter
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
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
