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Achondroplasia with the FGFR3 1138g→a (G380R) mutation in two sibs sharing a 4p haplotype derived from their unaffected father | Journal of Medical Genetics
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FGFR3 protein structure and reported locations of FGFR3 gene mutations... | Download Scientific Diagram
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Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report - Nagata - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset – ScienceOpen
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