Best Practices in PGT 2019 – Embryolab Academy
Speakers-2019 – Abilities Days
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
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
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
Loop | Georgios S Markopoulos
Ο Διευθυντής του εργαστηρίου... - ATG - Access To Genome | Facebook
ATG - Access To Genome - Posts | Facebook
Υπεύθυνοι Τμημάτων - ATG Διαγνωστικό κέντρο
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
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
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Γιάννης Παπουλίδης (@JonAPap) / Twitter
ΔΗΜΟΣΙΕΥΣΕΙΣ - ATG Πρότυπο Διαγνωστικό Κέντρο
Medicina | Free Full-Text | A New ABCA3 Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome
Molecular Cytogenetics Research Papers - Academia.edu
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
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
Speakers-2019 – Abilities Days
ΠΡΟΣΩΠΟ – Βιβλιοnet
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
