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Identification of the FGFR3G380R Mutant As a Likely Cause of Psychomotor Delay in an Achondroplastic Child: A Combined Clinical Exome Sequencing and Biomolecular Modeling Approach
 
 
Proceeding Paper

Article Versions Notes

Proceedings 2018, 2(13), 1002; https://doi.org/10.3390/proceedings2131002
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article pdf uploaded. 4 December 2018 12:29 CET Version of Record https://www.mdpi.com/2504-3900/2/13/1002/pdf
article html file updated 26 September 2022 11:00 CEST Original file https://www.mdpi.com/2504-3900/2/13/1002/html
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