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

Por Barik, Mayadhar, Bajpai, Minu, Malhotra, Arun, Samantaray, Jyotish Chandra, Dwivedi, Sadananda, Das, Sambhunath
Publicado no J Pediatr Neurosci (2015)

Genome-Wide Association Study in Craniosynostosis Condition Using Innovative Systematic Bioinformatic Analysis Tools and Techniques: Future Prospective and Clinical Practice

Por Barik, Mayadhar, Bajpai, Minu, Malhotra, Arun, Samantaray, Jyotish C., Dwivedi, Sadananda, Das, Sambhunath
Publicado no J Pediatr Neurosci (2018)