Ιωάννης Βαρβάκης - Βικιπαίδεια
Γιάννης Παπουλίδης Archives - Ο Ντελάλης
Loop | Georgios S Markopoulos
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
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
A novel familial mutation associated with Treacher Collins syndrome: A case report
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
ΠΡΟΣΩΠΟ – Βιβλιοnet
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Prenatal diagnosis of Baraitser – Winter syndrome using exome sequencing: Clinical report and review of literature - ScienceDirect
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
Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Ευεργέτες δύο πατρίδων, Ιωάννης Βαρβάκης (1750-1824), Δημήτριος Μπερναδράκης (1799-1870), Γρηγόριος Μαρασλής (1831-1907) - Κωνσταντίνος Κ. Παπουλίδης | Skroutz.gr
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
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
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
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ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
Best Practices in PGT 2019 – Embryolab Academy
Medicina | Free Full-Text | A New ABCA3 Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome
OLD FOOTBALL - Εμφάνιση άρθρων βάσει ετικέτας: Παπουλίδης Γιάννης
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library
