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Annales De Biologie Clinique|August 7, 2018
[The suitable prescription of the thyroid blood test in the diagnosis of dysthyroidism: a retrospective study in Rouen University Hospital]Fiston Kasonga, Kevin Cassinari, Valéry Brunel, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|March 12, 2025
First prenatal case of jumping-like translocations: unraveling complex chromosomal rearrangementsKevin Cassinari, Anne Claire Brehin, Ferdi Kundul, et al.
Familial Cancer|October 29, 2017
Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer geneticsGaëlle Collet, Nathalie Parodi, Kevin Cassinari, et al.
Journal of Alzheimer'S Disease : JAD|March 26, 2019
Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer's DiseaseEmmanuelle Boscher, Thomas Husson, Olivier Quenez, et al.
Acta Neuropathologica Communications|April 19, 2020
Simultaneous detection of EGFR amplification and EGFRvIII variant using digital PCR-based method in glioblastomaMaxime Fontanilles, Florent Marguet, Philippe Ruminy, et al.
Translational Psychiatry|February 26, 2020
Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical useThomas Husson, François Lecoquierre, Kevin Cassinari, et al.
Human Mutation|June 24, 2019
Identification of mobile retrocopies during genetic testing: Consequences for routine diagnosisNicolas Chatron, Kevin Cassinari, Olivier Quenez, et al.
European Journal of Human Genetics : EJHG|June 28, 2020
Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluationOlivier Quenez, Kevin Cassinari, Sophie Coutant, et al.
Alzheimer'S Research & Therapy|May 11, 2023
Phenotype and imaging features associated with APP duplicationsLou Grangeon, Camille Charbonnier, Aline Zarea, et al.
European Journal of Human Genetics : EJHG|April 4, 2025
Reanalysis of unsolved prenatal exome sequencing for structural defects: diagnostic yield and contribution of postnatal/postmortem featuresChristel Thauvin-Robinet, Aurore Garde, Maud Favier, et al.
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