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Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm

Detalles Bibliográficos
Autores principales: Gnoli, Maria, Pedrini, Elena, Mordenti, Marina, Tremosini, Morena, Sangiorgi, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132357/
http://dx.doi.org/10.1186/1824-7288-40-S1-A8
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author Gnoli, Maria
Pedrini, Elena
Mordenti, Marina
Tremosini, Morena
Sangiorgi, Luca
author_facet Gnoli, Maria
Pedrini, Elena
Mordenti, Marina
Tremosini, Morena
Sangiorgi, Luca
author_sort Gnoli, Maria
collection PubMed
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spelling pubmed-41323572014-08-19 Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm Gnoli, Maria Pedrini, Elena Mordenti, Marina Tremosini, Morena Sangiorgi, Luca Ital J Pediatr Meeting Abstract BioMed Central 2014-08-11 /pmc/articles/PMC4132357/ http://dx.doi.org/10.1186/1824-7288-40-S1-A8 Text en Copyright © 2014 Gnoli et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Meeting Abstract
Gnoli, Maria
Pedrini, Elena
Mordenti, Marina
Tremosini, Morena
Sangiorgi, Luca
Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm
title Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm
title_full Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm
title_fullStr Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm
title_full_unstemmed Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm
title_short Skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. Hereditary multiple Osteochondromas as example/paradigm
title_sort skeletal dysplasias: approach to the clinical diagnosis and implication of appropriate diagnosis for knowledge and research studies in these rare diseases. hereditary multiple osteochondromas as example/paradigm
topic Meeting Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132357/
http://dx.doi.org/10.1186/1824-7288-40-S1-A8
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