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bibliographicCitation Santos HG, Almeida M, Fernandes H, Wilkie AO, Wilkie A. Clinical hypochondroplasia in a family caused by a heterozygous double mutation in FGFR3 encoding GLY380LYS. Am J Med Genet A. 2007 Feb 15;143(4):355–9. doi: 10.1002/ajmg.a.31556. PMID: 17256796.
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title Clinical hypochondroplasia in a family caused by a heterozygous double mutation in FGFR3 encoding GLY380LYS
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