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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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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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Novel fibroblast growth factor receptor 3 (FGFR3) mutations in bladder cancer previously identified in non-lethal skeletal disorders | European Journal of Human Genetics
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FGFR3 targeting strategies for achondroplasia | Expert Reviews in Molecular Medicine | Cambridge Core
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Novel fibroblast growth factor receptor 3 (FGFR3) mutations in bladder cancer previously identified in non-lethal skeletal disorders | European Journal of Human Genetics
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Genes | Free Full-Text | Detection of G1138A Mutation of the FGFR3 Gene in Tooth Material from a 180-Year-Old Museological Achondroplastic Skeleton
Meclozine Facilitates Proliferation and Differentiation of Chondrocytes by Attenuating Abnormally Activated FGFR3 Signaling in Achondroplasia | PLOS ONE
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An FGFR3/MYC positive feedback loop provides new opportunities for targeted therapies in bladder cancers | EMBO Molecular Medicine
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Results of the FGFR3 gene analysis. A heterozygous A1949C (black arrow)... | Download Scientific Diagram
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FGFR3 protein structure and reported locations of FGFR3 gene mutations... | Download Scientific Diagram
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