Further delineation of the NTHL1 associated syndrome: a report from the French oncogenetic consortium

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TitreFurther delineation of the NTHL1 associated syndrome: a report from the French oncogenetic consortium
Type de publicationJournal Article
Year of Publication2020
AuteursBoulouard F., Kasper E., Buisine M., Lienard G., Vasseur S., Manase S., Bahuau M., Bubien V., Coulet F., Cusin V., Dhooge M., Golmard L., Goussot V., Hamzaoui N., Lacaze E., Lejeune S., Mauillon J., Pinson S., Tlemsani C., Toulas C., Rey J., Uhrhammer N., Bougeard-Denoyelle G., Frebourg T., Houdayer C., Baert-Desurmont S.
JournalEUROPEAN JOURNAL OF HUMAN GENETICS
Volume28
Pagination543
Date PublishedDEC
Type of ArticleMeeting Abstract
ISSN1018-4813