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Athina Theodosiou

Showing results (1-10 of 19) with videos related to

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Bioinformatics (Oxford, England)|December 27, 2011
LaTcOm: a web server for visualizing rare codon clusters in coding sequencesAthina Theodosiou, Vasilis J Promponas
Molecular Biology and Evolution|April 17, 2009
Evolutionary scenarios of Notch proteinsAthina Theodosiou, Stilianos Arhondakis, Marc Baumann, et al.
Molecular Cytogenetics|June 23, 2018
Cryptic breakpoint identified by whole-genome mate-pair sequencing in a rare paternally inherited complex chromosomal rearrangementConstantia Aristidou, Athina Theodosiou, Andria Ketoni, et al.
Heliyon|December 21, 2023
CHD2 pathogenic nonsense variant in a three-generation family with variable phenotype and a paracentric inversion 16: Case reportEleni Angelopoulou, Athina Theodosiou, Ioannis Papaevripidou, et al.
Clinical Case Reports|March 9, 2019
De novo mosaic <i>MECP2</i> mutation in a female with Rett syndromeAngelos Alexandrou, Ioannis Papaevripidou, Ioanna Maria Alexandrou, et al.
European Journal of Medical Genetics|May 4, 2020
First reported case of Steel syndrome in the European population: A novel homozygous mutation in COL27A1 and review of the literatureEvie Kritioti, Athina Theodosiou, Nayia Nicolaou, et al.
Database : the Journal of Biological Databases and Curation|April 18, 2012
The PRINTS database: a fine-grained protein sequence annotation and analysis resource--its status in 2012Teresa K Attwood, Alain Coletta, Gareth Muirhead, et al.
Plos One|January 11, 2017
Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair SequencingConstantia Aristidou, Costas Koufaris, Athina Theodosiou, et al.
Genes|January 21, 2023
Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome SequencingConstantia Aristidou, Athina Theodosiou, Angelos Alexandrou, et al.
Plos One|July 29, 2021
Unravelling the genetic causes of multiple malformation syndromes: A whole exome sequencing study of the Cypriot populationEvie Kritioti, Athina Theodosiou, Thibaud Parpaite, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|December 27, 2011
LaTcOm: a web server for visualizing rare codon clusters in coding sequencesAthina Theodosiou, Vasilis J Promponas
Molecular Biology and Evolution|April 17, 2009
Evolutionary scenarios of Notch proteinsAthina Theodosiou, Stilianos Arhondakis, Marc Baumann, et al.
Molecular Cytogenetics|June 23, 2018
Cryptic breakpoint identified by whole-genome mate-pair sequencing in a rare paternally inherited complex chromosomal rearrangementConstantia Aristidou, Athina Theodosiou, Andria Ketoni, et al.
Heliyon|December 21, 2023
CHD2 pathogenic nonsense variant in a three-generation family with variable phenotype and a paracentric inversion 16: Case reportEleni Angelopoulou, Athina Theodosiou, Ioannis Papaevripidou, et al.
Clinical Case Reports|March 9, 2019
De novo mosaic <i>MECP2</i> mutation in a female with Rett syndromeAngelos Alexandrou, Ioannis Papaevripidou, Ioanna Maria Alexandrou, et al.
European Journal of Medical Genetics|May 4, 2020
First reported case of Steel syndrome in the European population: A novel homozygous mutation in COL27A1 and review of the literatureEvie Kritioti, Athina Theodosiou, Nayia Nicolaou, et al.
Database : the Journal of Biological Databases and Curation|April 18, 2012
The PRINTS database: a fine-grained protein sequence annotation and analysis resource--its status in 2012Teresa K Attwood, Alain Coletta, Gareth Muirhead, et al.
Plos One|January 11, 2017
Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair SequencingConstantia Aristidou, Costas Koufaris, Athina Theodosiou, et al.
Genes|January 21, 2023
Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome SequencingConstantia Aristidou, Athina Theodosiou, Angelos Alexandrou, et al.
Plos One|July 29, 2021
Unravelling the genetic causes of multiple malformation syndromes: A whole exome sequencing study of the Cypriot populationEvie Kritioti, Athina Theodosiou, Thibaud Parpaite, et al.
Pageof 2