Mutational identification of fibroblast growth factor receptor 1 and fibroblast growth factor receptor 2 genes in craniosynostosis in Indian population

OBJECTIVE: The Objective of this study was to identify the association of mutation of fibroblast growth factor receptor 1 (FGFR1), FGFR2 genes with syndromic as well as non-syndromic craniosynostosis in Indian population. MATERIALS AND METHODS: Retrospective analysis of our records from January 2008...

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Detalles Bibliográficos
Autores principales: Pandey, Rajeev Kumar, Bajpai, Minu, Ali, Abid, Gayan, Sukanya, Singh, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897141/
https://www.ncbi.nlm.nih.gov/pubmed/24497711
http://dx.doi.org/10.4103/0971-6866.124374

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897141/
https://www.ncbi.nlm.nih.gov/pubmed/24497711
http://dx.doi.org/10.4103/0971-6866.124374

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