Novel mutation detection of fibroblast growth factor receptor 1 (FGFR1) gene, FGFR2IIIa, FGFR2IIIb, FGFR2IIIc, FGFR3, FGFR4 gene for craniosynostosis: A prospective study in Asian Indian patient

BACKGROUND: Craniosynostosis (CS) syndrome is an autosomal dominant condition classically combining craniosynostosis and non-syndromic craniosynostosis with digital anomalies of the hands and feet. The majority of cases are caused by heterozygous mutations in the third immunoglobulin-like domain (Ig...

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Detalhes bibliográficos
Publicado no:J Pediatr Neurosci
Main Authors: Barik, Mayadhar, Bajpai, Minu, Malhotra, Arun, Samantaray, Jyotish Chandra, Dwivedi, Sadananda, Das, Sambhunath
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2015
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4611887/
https://ncbi.nlm.nih.gov/pubmed/26557159
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.165659
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