OLD FOOTBALL - Εμφάνιση άρθρων βάσει ετικέτας: Παπουλίδης Γιάννης
Loop | IOANNIS PAPOULIDIS
Speakers-2019 – Abilities Days
Συμβουλευτική στο ελεύθερο εμβρυικό DNA: «Λοιπά γενετικά σύνδρομα» – Ελληνική Εταιρία Εμβρυομητρικής Ιατρικής
Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο
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
Γιάννης Παπουλίδης Archives - Ο Ντελάλης
Best Practices in PGT 2019 – Embryolab Academy
ATG - Access To Genome - Posts | Facebook
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
Ιωάννης Βαρβάκης - Βικιπαίδεια
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
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
Loop | Georgios S Markopoulos
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
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
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 - Senior Funds Accountant - Alter Domus | LinkedIn
Prenatal diagnosis of Baraitser – Winter syndrome using exome sequencing: Clinical report and review of literature - ScienceDirect
