Familial hypochondroplasia and acanthosis nigricans with FGFR3 K650T mutation
Cossiez Cacard, M.A., Coulombe, J., Bernard, P., Kaci, N., Bressieux, J.M., Souchon, P.F., Motte, J., Legeai-Mallet, L., Hadj-Rabia, S., Eschard, C.Volume:
30
Language:
english
Journal:
Journal of the European Academy of Dermatology and Venereology
DOI:
10.1111/jdv.13061
Date:
May, 2016
File:
PDF, 180 KB
english, 2016