ΠΡΟΣΩΠΟ – Βιβλιοnet
Speakers-2019 – Abilities Days
ATG - Access To Genome - Photos | Facebook
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Speakers-2019 – Abilities Days
Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο
ATG - Access To Genome - Posts | Facebook
Ioannis Papoulidis - Senior Funds Accountant - Alter Domus | LinkedIn
Prenatal diagnosis of Baraitser – Winter syndrome using exome sequencing: Clinical report and review of literature - ScienceDirect
Molecular Cytogenetics Research Papers - Academia.edu
A novel familial mutation associated with Treacher Collins syndrome: A case report
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
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
Συμβουλευτική στο ελεύθερο εμβρυικό DNA: «Λοιπά γενετικά σύνδρομα» – Ελληνική Εταιρία Εμβρυομητρικής Ιατρικής
Ιωάννης Βαρβάκης - Βικιπαίδεια
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
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Γιάννης Παπουλίδης Archives - Ο Ντελάλης
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
OLD FOOTBALL - Εμφάνιση άρθρων βάσει ετικέτας: Παπουλίδης Γιάννης
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
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
