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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
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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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 |
description | |
format | Online Article Text |
id | pubmed-4132357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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