Ngoc, N., & 		Duc, H.
(2023).
 Detection of the de novo Pro253Arg Mutation of Fibroblast Growth Factor Receptor 2 (FGFR2) in a Pediatric Patient with Congenital Hand Anomaly.
<em>VNU Journal Of Science: Natural Sciences And Technology, 40</em>(1).
doi:10.25073/2588-1140/vnunst.5583