Resultats de la cerca - Viviane Baral
- Mostrar 1 - 3 resultats de 3
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Deletions at the SOX10 Gene Locus Cause Waardenburg Syndrome Types 2 and 4 per Nadège Bondurand, Florence Dastot‐Le Moal, Laure Stanchina, Nathalie Collot, Viviane Baral, Sandrine Marlin, Tania Attié‐Bitach, Irina Giurgea, Laurent Skopinski, William Reardon, Annick Toutain, Pierre Sarda, Echaieb Anis, Marilyn Lackmy-Port-Lis, Renaud Touraine, Jeanne Amiel, Michel Goossens, Véronique Pingault
Publicat 2007Artigo -
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Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness per Véronique Pingault, Virginie Bodereau, Viviane Baral, Séverine Marcos, Yuli Watanabe, Asma Chaoui, Corinne Fouveaut, Chrystel Leroy, O. Vérier‐Mine, Christine Francannet, Delphine Dupin‐Deguine, F. Archambeaud, François-Joseph Kurtz, Jacques Young, Jérôme Bertherat, Sandrine Marlin, Michel Goossens, Jean‐Pierre Hardelin, Catherine Dodé, Nadège Bondurand
Publicat 2013Artigo
Eines de cerca:
Matèries relacionades
Biology
Genetics
Neural crest
SOX10
Gene
Phenotype
Waardenburg syndrome
Cell biology
Complementation
Coronavirus disease 2019 (COVID-19)
Disease
Embryo
Endocrinology
Infectious disease (medical specialty)
Internal medicine
Kallmann syndrome
Locus (genetics)
Medicine
Missense mutation
Mutant
Mutation