Resultats de la cerca - Mylène Valduga
- Mostrar 1 - 2 resultats de 2
-
1
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study per 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
Publicat 2017Artigo -
2
A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH per Céline Poirsier, Justine Besseau-Ayasse, Caroline Schluth–Bolard, Jérôme Toutain, Chantal Missirian, Cédric Le Caignec, Anne Bazin, Marie Christine de Blois, Paul Kuentz, Marie Catty, Agnès Choiset, Ghislaine Plessis, Audrey Basinko, Pascaline Létard, Elisabeth Flori, Mélanie Jimenez, Mylène Valduga, Emilie Landais, Hakima Lallaoui, François Cartault, James Lespinasse, Dominique Martin–Coignard, Patrick Callier, Céline Pebrel‐Richard, Marie-France Portnoı̈, Tiffany Busa, Aline Receveur, Florence Amblard, Catherine Yardin, Radu Harbuz, Fabienne Prieur, Nathalie Le Meur, Eva Pipiras, Pascale Kleinfinger, François Vialard, Martine Doco‐Fenzy
Publicat 2015Artigo
Eines de cerca:
Matèries relacionades
Biology
Chromosome
Copy-number variation
Fetus
Gene
Genetics
Genome
Medicine
Pathology
Pregnancy
Prenatal diagnosis
Retrospective cohort study
Aneuploidy
Clinical significance
Comparative genomic hybridization
Cytogenetics
Environmental health
Etiology
Gene expression
Internal medicine
Karyotype
Medical diagnosis
Microarray
Microarray analysis techniques
Microdeletion syndrome
Pediatrics
Phenotype
Population