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Author/Creator Mitrakos, Anastasios

1. Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms. (2nd January 2023)

Authors:
Veltra, Danai; Tilemis, Faidon-Nikolaos; Marinakis, Nikolaos M.; Svingou, Maria; Mitrakos, Anastasios; Kosma, Konstantina; Tsoutsou, Irene; Makrythanasis, Periklis; Theodorou, Virginia; Katsalouli, Marina; Vorgia, Pelagia; Niotakis, Georgios; Vartzelis, Georgios; Dinopoulos, Argirios; Evangeliou,...
Journal:
Expert review of molecular diagnostics
Issue:
Volume 23:Number 1(2023)
Page Start:
85
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Compound heterozygosity of a paternal submicroscopic deletion and a maternal missense mutation in POR gene: Antley‐bixler syndrome phenotype in three sibling fetuses. Issue 7 (11th March 2016)

Authors:
Tzetis, Maria; Konstantinidou, Anastasia; Sofocleous, Christalena; Kosma, Konstantina; Mitrakos, Anastasios; Tzannatos, Christina; Kitsiou‐Tzeli, Sofia
Journal:
Birth defects research
Issue:
Volume 106:Issue 7(2016)
Page Start:
536
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗