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
_version_ 1782445268538490880
author Nagahara, Keiko
Harada, Yuki
Futami, Tohru
Takagi, Masaki
Nishimura, Gen
Hasegawa, Yukihiro
author_facet Nagahara, Keiko
Harada, Yuki
Futami, Tohru
Takagi, Masaki
Nishimura, Gen
Hasegawa, Yukihiro
author_sort Nagahara, Keiko
collection PubMed
description
format Online
Article
Text
id pubmed-4965510
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher The Japanese Society for Pediatric Endocrinology
record_format MEDLINE/PubMed
spelling pubmed-49655102016-08-09 A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3 Nagahara, Keiko Harada, Yuki Futami, Tohru Takagi, Masaki Nishimura, Gen Hasegawa, Yukihiro Clin Pediatr Endocrinol Mutation-in-Brief The Japanese Society for Pediatric Endocrinology 2016-07-20 2016-07 /pmc/articles/PMC4965510/ /pubmed/27507911 http://dx.doi.org/10.1297/cpe.25.103 Text en 2016©The Japanese Society for Pediatric Endocrinology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Mutation-in-Brief
Nagahara, Keiko
Harada, Yuki
Futami, Tohru
Takagi, Masaki
Nishimura, Gen
Hasegawa, Yukihiro
A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3
title A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3
title_full A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3
title_fullStr A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3
title_full_unstemmed A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3
title_short A Japanese familial case of hypochondroplasia with a novel mutation in FGFR3
title_sort japanese familial case of hypochondroplasia with a novel mutation in fgfr3
topic Mutation-in-Brief
url 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
work_keys_str_mv AT nagaharakeiko ajapanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT haradayuki ajapanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT futamitohru ajapanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT takagimasaki ajapanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT nishimuragen ajapanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT hasegawayukihiro ajapanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT nagaharakeiko japanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT haradayuki japanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT futamitohru japanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT takagimasaki japanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT nishimuragen japanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3
AT hasegawayukihiro japanesefamilialcaseofhypochondroplasiawithanovelmutationinfgfr3

Ejemplares similares