Prenatal diagnosis of Baraitser – Winter syndrome using exome sequencing: Clinical report and review of literature - ScienceDirect
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Molecular Cytogenetics Research Papers - Academia.edu
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Συμβουλευτική στο ελεύθερο εμβρυικό DNA: «Λοιπά γενετικά σύνδρομα» – Ελληνική Εταιρία Εμβρυομητρικής Ιατρικής
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Medicina | Free Full-Text | A New ABCA3 Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
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
Ioannis Papoulidis - Senior Funds Accountant - Alter Domus | LinkedIn
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
OLD FOOTBALL - Εμφάνιση άρθρων βάσει ετικέτας: Παπουλίδης Γιάννης
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Speakers-2019 – Abilities Days
A novel familial mutation associated with Treacher Collins syndrome: A case report
Loop | Georgios S Markopoulos
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
Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
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Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
