Apert Syndrome with Preaxial Polydactyly with FGFR2 Gene Mutation
Manisha Goyal1, Ashok Gupta2, Seema Kapoor3
1Centre of Rare Disease, Department of Pediatrics, J K Lone Hospital, SMS Medical College, Jaipur, Rajasthan, India. manidr2000@gmail.com.
Indian Journal of Pediatrics
|December 28, 2019
Abstract
No abstract available in PubMed .
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