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Eftychia Dimitriadou

Showing results (1-10 of 26) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|September 17, 2015
Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome AmplificationEftychia Dimitriadou, Masoud Zamani Esteki, Joris Robert Vermeesch
Molecular Cytogenetics|July 31, 2014
Single cell segmental aneuploidy detection is compromised by S phaseEftychia Dimitriadou, Niels Van der Aa, Jiqiu Cheng, et al.
Journal of Assisted Reproduction and Genetics|January 4, 2024
Exploring attitudes and experiences with reproductive genetic carrier screening among couples seeking medically assisted reproduction: a longitudinal survey studyEva Van Steijvoort, Mathilde Cassou, Camille De Schutter, et al.
The Journal of Allergy and Clinical Immunology. in Practice|December 26, 2024
Preimplantation genetic testing for hereditary angioedema as a potential dominant cost-effective interventionWillem Roosens, Lore Lannoo, Ellen Denayer, et al.
Human Molecular Genetics|January 17, 2009
Retrotransposon RNA expression and evidence for retrotransposition events in human oocytesIoannis Georgiou, Dimitrios Noutsopoulos, Eftychia Dimitriadou, et al.
Cytogenetic and Genome Research|April 8, 2016
Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal ParentsWolfram Demaerel, Majid Hosseinzadeh, Nayereh Nouri, et al.
Human Reproduction Open|June 6, 2020
ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders, Filipa Carvalho, Céline Moutou, et al.
Human Reproduction Open|June 6, 2020
ESHRE PGT Consortium good practice recommendations for the detection of structural and numerical chromosomal aberrations, Edith Coonen, Carmen Rubio, et al.
Nucleic Acids Research|February 25, 2022
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencingHeleen Masset, Jia Ding, Eftychia Dimitriadou, et al.
European Journal of Medical Genetics|September 24, 2009
Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1Bernard Thienpont, Eftychia Dimitriadou, Katerina Theodoropoulos, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|September 17, 2015
Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome AmplificationEftychia Dimitriadou, Masoud Zamani Esteki, Joris Robert Vermeesch
Molecular Cytogenetics|July 31, 2014
Single cell segmental aneuploidy detection is compromised by S phaseEftychia Dimitriadou, Niels Van der Aa, Jiqiu Cheng, et al.
Journal of Assisted Reproduction and Genetics|January 4, 2024
Exploring attitudes and experiences with reproductive genetic carrier screening among couples seeking medically assisted reproduction: a longitudinal survey studyEva Van Steijvoort, Mathilde Cassou, Camille De Schutter, et al.
The Journal of Allergy and Clinical Immunology. in Practice|December 26, 2024
Preimplantation genetic testing for hereditary angioedema as a potential dominant cost-effective interventionWillem Roosens, Lore Lannoo, Ellen Denayer, et al.
Human Molecular Genetics|January 17, 2009
Retrotransposon RNA expression and evidence for retrotransposition events in human oocytesIoannis Georgiou, Dimitrios Noutsopoulos, Eftychia Dimitriadou, et al.
Cytogenetic and Genome Research|April 8, 2016
Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal ParentsWolfram Demaerel, Majid Hosseinzadeh, Nayereh Nouri, et al.
Human Reproduction Open|June 6, 2020
ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders, Filipa Carvalho, Céline Moutou, et al.
Human Reproduction Open|June 6, 2020
ESHRE PGT Consortium good practice recommendations for the detection of structural and numerical chromosomal aberrations, Edith Coonen, Carmen Rubio, et al.
Nucleic Acids Research|February 25, 2022
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencingHeleen Masset, Jia Ding, Eftychia Dimitriadou, et al.
European Journal of Medical Genetics|September 24, 2009
Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1Bernard Thienpont, Eftychia Dimitriadou, Katerina Theodoropoulos, et al.
Pageof 3