DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Winterpacht A, Hilbert K, Stelzer C. , et al.
A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasia.
Physiol Genomics 2000;
2 (01) 9-12
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