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Ευεργέτες δύο πατρίδων, Ιωάννης Βαρβάκης (1750-1824), Δημήτριος  Μπερναδράκης (1799-1870), Γρηγόριος Μαρασλής (1831-1907) - Κωνσταντίνος Κ.  Παπουλίδης | Skroutz.gr
Ευεργέτες δύο πατρίδων, Ιωάννης Βαρβάκης (1750-1824), Δημήτριος Μπερναδράκης (1799-1870), Γρηγόριος Μαρασλής (1831-1907) - Κωνσταντίνος Κ. Παπουλίδης | Skroutz.gr

Best Practices in PGT 2019 – Embryolab Academy
Best Practices in PGT 2019 – Embryolab Academy

Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki

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
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

Medicina | Free Full-Text | A New ABCA3 Gene Mutation c.3445G>A  (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress  Syndrome
Medicina | Free Full-Text | A New ABCA3 Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome

Ιωάννης Βαρβάκης - Βικιπαίδεια
Ιωάννης Βαρβάκης - Βικιπαίδεια

Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. |  LinkedIn
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn

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
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

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
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 - Lab Manager -Director - Access To Genome - ATG P.C. |  LinkedIn
Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. | LinkedIn

ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη

Ioannis Papoulidis - Lab Manager -Director - Access To Genome - ATG P.C. |  LinkedIn
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
Medicina | Free Full-Text | A New ABCA3 Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome

A novel familial mutation associated with Treacher Collins syndrome: A case  report
A novel familial mutation associated with Treacher Collins syndrome: A case report

ΔΗΜΟΣΙΕΥΣΕΙΣ - ATG Πρότυπο Διαγνωστικό Κέντρο
ΔΗΜΟΣΙΕΥΣΕΙΣ - ATG Πρότυπο Διαγνωστικό Κέντρο

Loop | Georgios S Markopoulos
Loop | Georgios S Markopoulos

ΠΡΟΣΩΠΟ – Βιβλιοnet
ΠΡΟΣΩΠΟ – Βιβλιοnet

Speakers-2019 – Abilities Days
Speakers-2019 – Abilities Days

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by  array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library

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 (@JonAPap) / Twitter
Γιάννης Παπουλίδης (@JonAPap) / Twitter

ATG - Access To Genome - Posts | Facebook
ATG - Access To Genome - Posts | Facebook

ATG - Access To Genome - Photos | Facebook
ATG - Access To Genome - Photos | Facebook

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
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

Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki
Ioannis PAPOULIDIS | Founder/Director | EuroGenetica S.A., Thessaloníki