Որոնման արդյունքները - Bérenice Herve
- Ցուցադրվում են 1 - 2 արդյունքները 2
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1
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study Matthieu Egloff, Bérenice Herve, T. Quibel, Sylvie Jaillard, G. Le Bouar, Kévin Uguen, A.‐H. Saliou, Mylène Valduga, E. Perdriolle, Charles Coutton, Anne-Laure Coston, Aurélie Coussement, Olivia Anselem, Chantal Missirian, Florence Bretelle, Fabienne Prieur, C. Fanget, Christine Muti, M.‐C. Jacquemot, Claire Bénéteau, Claudine Le Vaillant, Michel Vekemans, Laurent Salomon, François Vialard, Valérie Malan
Հրապարակվել է 2017Artigo -
2
Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases Quentin Testard, Xavier Vanhoye, Kévin Yauy, Marie-Emmanuelle Naud, Gaëlle Vieville, Francis Rousseau, Benjamin Dauriat, Valentine Marquet, Sylvie Bourthoumieu, David Geneviève, Vincent Gâtinois, Constance Wells, Marjolaine Willems, Christine Coubes, Lucile Pinson, Rodolphe Dard, Aude Tessier, Bérenice Herve, François Vialard, Inès Harzallah, Renaud Touraine, Benjamin Cogné, Wallid Deb, Thomas Besnard, Olivier Pichon, Béatrice Laudier, Laurent Mesnard, Alice Doreille, Tiffany Busa, Chantal Missirian, Véronique Satre, Charles Coutton, Tristan Celse, Radu Harbuz, Laure Raymond, Jean-François Taly, Julien Thévenon
Հրապարակվել է 2022Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Copy-number variation
Gene
Genetics
Genome
Medicine
Retrospective cohort study
Aneuploidy
Bioinformatics
Chromosome
Clinical significance
Cohort
Etiology
Exome
Exome sequencing
Fetus
Gene expression
Internal medicine
Karyotype
Medical genetics
Microarray
Microarray analysis techniques
Mutation
Oncology
Pathology
Pregnancy
Prenatal diagnosis
Prospective cohort study