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A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1

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Dades bibliogràfiques
Publicat a:Clin Pediatr Endocrinol
Autors principals: Higuchi, Shinji, Takagi, Masaki, Shimomura, Satoshi, Nishimura, Gen, Hasegawa, Yukihiro
Format: Artigo
Idioma:Inglês
Publicat: The Japanese Society for Pediatric Endocrinology 2016
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4965511/
https://ncbi.nlm.nih.gov/pubmed/27507912
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.25.107
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