অনুসন্ধান ফলাফলগুলি - Christel Vaché
- প্রদর্শন 1 - 7 ফলাফল এর 7
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Experience of targeted Usher exome sequencing as a clinical test অনুযায়ী Thomas Besnard, Gema García‐García, David Baux, Christel Vaché, Valérie Faugère, Lise Larrieu, Susana Léonard, José M. Millán, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux
প্রকাশিত 2013Artigo -
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Enrichment of LOVD-USHbases with 152<i>USH2A</i>Genotypes Defines an Extensive Mutational Spectrum and Highlights Missense Hotspots অনুযায়ী David Baux, Catherine Blanchet, Christian Hamel, Isabelle Meunier, Lise Larrieu, Valérie Faugère, Christel Vaché, Pierangela Castorina, Bernard Puech, Dominique Bonneau, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux
প্রকাশিত 2014Artigo -
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Non-USH2A mutations in USH2 patients অনুযায়ী Thomas Besnard, Christel Vaché, David Baux, Lise Larrieu, Caroline Abadie, Catherine Blanchet, Sylvie Odent, Patricia Blanchet, Patrick Calvas, Christian Hamel, Hélène Dollfus, Geneviève Lina‐Granade, James Lespinasse, Albert David, Bertrand Isidor, G Morin, Sue Malcolm, Sylvie Tuffery‐Giraud, Mireille Claustres, Anne‐Françoise Roux
প্রকাশিত 2011Artigo -
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Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation অনুযায়ী Radulfus WN Slijkerman, Christel Vaché, Margo Dona, Gema García‐García, Mireille Claustres, Lisette Hetterschijt, Theo Peters, Bas P. Hartel, Ronald J. E. Pennings, José M Millan, Elena Aller, Alejandro Garanto, Rob W.J. Collin, Hannie Kremer, Anne‐Françoise Roux, Erwin van Wijk
প্রকাশিত 2016Artigo -
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SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect অনুযায়ী Alisdair McNeill, Emanuela Iovino, Luke Mansard, Christel Vaché, David Baux, Emma Bedoukian, Helen Cox, John Dean, David Goudie, Ajith Kumar, Ruth Newbury‐Ecob, Chiara Fallerini, Alessandra Renieri, Diego Lopergolo, Francesca Mari, Catherine Blanchet, Marjolaine Willems, Anne‐Françoise Roux, Tommaso Pippucci, Eric Delpire
প্রকাশিত 2020Artigo -
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Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients অনুযায়ী David Baux, Christel Vaché, Christophe Blanchet, Marjolaine Willems, C. Baudoin, Mélodie Moclyn, Valérie Faugère, Renaud Touraine, Bertrand Isidor, Delphine Dupin‐Deguine, Mathilde Nizon, Marie Vincent, Sandra Mercier, C. Calais, Gema García‐García, Zohor A. Azher, Linda M. Lambert, Y. Perdomo-Trujillo, Fabienne Giuliano, Mireille Claustres, M. Kœnig, Michel Mondain, Anne‐Françoise Roux
প্রকাশিত 2017Artigo
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
Biology
Gene
Genetics
Mutation
Retinitis pigmentosa
Medicine
Minigene
RNA
RNA splicing
Usher syndrome
Audiology
Bioinformatics
Computational biology
Exome sequencing
Genetic heterogeneity
Hearing loss
Missense mutation
Phenotype
Alternative splicing
Cohort
Corticogenesis
DNA sequencing
Deep sequencing
Embryonic stem cell
Exome
Exon
Gene isoform
Genome
Genotype
Habilitation