학술논문
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium
Document Type
Article
Author
Boulouard, F.; Kasper, E.; Lienard, G.; Vasseur, S.; Manase, S.; Mauillon, J.; Bougeard, G.; Frebourg, T.; Houdayer, C.; Baert-Desurmont, S.; Buisine, M.-P.; Bahuau, M.; Barouk Simonet, E.; Bubien, V.; Coulet, F.; Cusin, V.; Dhooge, M.; Golmard, L.; Goussot, V.; Hamzaoui, N.; Tlemsani, C.; Lacaze, E.; Lejeune, S.; Beaumont, M.-P.; Pinson, S.; Toulas, C.; Rey, J.-M.; Uhrhammer, N.
Source
In: Clinical Genetics . (Clinical Genetics, May 2021, 99(5):662-672)
Subject
Language
English
ISSN
13990004
00099163
00099163