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Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.

Detalles Bibliográficos
Autores principales: Hughes, J., Nevin, N. C., Morrison, P. J.
Formato: Texto
Lenguaje:English
Publicado: Ulster Medical Society 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2449219/
https://www.ncbi.nlm.nih.gov/pubmed/11428324
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author Hughes, J.
Nevin, N. C.
Morrison, P. J.
author_facet Hughes, J.
Nevin, N. C.
Morrison, P. J.
author_sort Hughes, J.
collection PubMed
description
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language English
publishDate 2001
publisher Ulster Medical Society
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spelling pubmed-24492192008-07-10 Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene. Hughes, J. Nevin, N. C. Morrison, P. J. Ulster Med J Research Article Ulster Medical Society 2001-05 /pmc/articles/PMC2449219/ /pubmed/11428324 Text en
spellingShingle Research Article
Hughes, J.
Nevin, N. C.
Morrison, P. J.
Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.
title Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.
title_full Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.
title_fullStr Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.
title_full_unstemmed Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.
title_short Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.
title_sort familial craniosynostosis due to pro250arg mutation in the fibroblast growth factor receptor 3 gene.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2449219/
https://www.ncbi.nlm.nih.gov/pubmed/11428324
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AT morrisonpj familialcraniosynostosisduetopro250argmutationinthefibroblastgrowthfactorreceptor3gene