ΠΡΟΣΩΠΟ – Βιβλιοnet
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
Speakers-2019 – Abilities Days
Ευεργέτες δύο πατρίδων, Ιωάννης Βαρβάκης (1750-1824), Δημήτριος Μπερναδράκης (1799-1870), Γρηγόριος Μαρασλής (1831-1907) - Κωνσταντίνος Κ. Παπουλίδης | Skroutz.gr
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) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
OLD FOOTBALL - Εμφάνιση άρθρων βάσει ετικέτας: Παπουλίδης Γιάννης
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
Prenatal diagnosis of Baraitser – Winter syndrome using exome sequencing: Clinical report and review of literature - ScienceDirect
Γιάννης Παπουλίδης (@JonAPap) / Twitter
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
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
A novel familial mutation associated with Treacher Collins syndrome: A case report
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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
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
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn
Molecular Cytogenetics Research Papers - Academia.edu
