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

Detalles Bibliográficos
Autores principales:	Nagahara, Keiko, Harada, Yuki, Futami, Tohru, Takagi, Masaki, Nishimura, Gen, Hasegawa, Yukihiro
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Japanese Society for Pediatric Endocrinology 2016
Materias:	Mutation-in-Brief
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965510/ https://www.ncbi.nlm.nih.gov/pubmed/27507911 http://dx.doi.org/10.1297/cpe.25.103

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