DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Bellus GA, Spector EB, Speiser PW. , et al.
Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype.
Am J Hum Genet 2000;
67 (06) 1411-1421
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