A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3.

Nagahara, Keiko; Harada, Yuki; Futami, Tohru; Takagi, Masaki; Nishimura, Gen; Hasegawa, Yukihiro.

Afiliação

Nagahara K; Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan; Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan.
Harada Y; Department of Orthopedic Surgery, Shiga Medical Center for Children, Shiga, Japan.
Futami T; Department of Orthopedic Surgery, Shiga Medical Center for Children, Shiga, Japan.
Takagi M; Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Nishimura G; Department of Radiology, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.
Hasegawa Y; Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.

Clin Pediatr Endocrinol ; 25(3): 103-6, 2016 Jul.

Article em En | MEDLINE | ID: mdl-27507911