WNT10A mutations: refining genotype, phenotype, penetrance, clinical variability and inheritance manner

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TitreWNT10A mutations: refining genotype, phenotype, penetrance, clinical variability and inheritance manner
Type de publicationJournal Article
Year of Publication2019
AuteursPatat O., Bailleul-Forestier I., Plaisancie J., Bonneau D., Colin E., Colson C., Cordier M., Coubes C., Demurger F., Dieux-Coeslier A., Fradin M., Gerard M., Goldenberg A., Isidor B., Journel H., Lacombe D., Lebrun M., Martin-Coignard D., Nizon M., Odent S., Petit F., Philip N., Piard J., Piard J., Plessis G., Putoux A., Quelin C., Thevenon J., Toutain A., Vanleberghe C., Verloes A., Vincent-Delorme C., Capri Y., Vaysse F., Calvas P., Chassaing N.
JournalEUROPEAN JOURNAL OF HUMAN GENETICS
Volume27
Pagination1302-1303
Date PublishedOCT
Type of ArticleMeeting Abstract
ISSN1018-4813