A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3.
作者信息
Nagahara Keiko, Harada Yuki, Futami Tohru, Takagi Masaki, Nishimura Gen, Hasegawa Yukihiro
机构信息
Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan; Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan.
Department of Orthopedic Surgery, Shiga Medical Center for Children, Shiga, Japan.
出版信息
Clin Pediatr Endocrinol. 2016 Jul;25(3):103-6. doi: 10.1297/cpe.25.103. Epub 2016 Jul 20.
Abstract
摘要
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本文引用的文献
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