Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 single-nucleotide variant versus a 3q13.31 microdeletion including ZBTB20

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TitrePrimrose syndrome: a phenotypic comparison of patients with a ZBTB20 single-nucleotide variant versus a 3q13.31 microdeletion including ZBTB20
Type de publicationJournal Article
Year of Publication2019
AuteursJuven A., Nambot S., Piton A., Callier P., Philippe C., Jean-Marcais N., Munnich A., Rio M., Colleaux L., Rondeau S., Steffann J., Attie-Bitach T., Thomas S., S. Chehadeh E, C. Delorme V, Bouquillon S., Francannet C., Laffargue F., Gouas L., Blesson S., Lacombe D., Vincent M., Isidor B., Journel H., Thauvin C., Faivre L.
JournalEUROPEAN JOURNAL OF HUMAN GENETICS
Volume27
Pagination377-378
Date PublishedJUL
Type of ArticleMeeting Abstract
ISSN1018-4813