Acanthosis nigricans in a Japanese boy with hypochondroplasia due to a K650T mutation in FGFR3

Hiroki Hirai, Junpei Hamada, Kosei Hasegawa, Eiichi Ishii
  • Clinical Pediatric Endocrinology, January 2017, Japanese Society for Pediatric Endocrinology
  • DOI: 10.1297/cpe.26.223
The author haven't finished explaining this publicationThe author haven't finished explaining this publication
Read Publication

http://dx.doi.org/10.1297/cpe.26.223

The following have contributed to this page: Dr Kosei Hasegawa