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2019•The Indian Journal of PediatricsRequires access

Apert Syndrome with Preaxial Polydactyly with FGFR2 Gene Mutation

Manisha Goyal, Ashok Gupta, Seema Kapoor, Anu Bhandari

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Key concepts: Medicine, Apert syndrome, Polydactyly, Dysostosis, Mutation, Genetics, Gene, Pediatrics

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