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2. Genomic organization of the human fibroblast growth factor receptor 2 (FGFR2) gene and comparative analysis of the human FGFR gene family. Zhang Y; Gorry MC; Post JC; Ehrlich GD Gene; 1999 Apr; 230(1):69-79. PubMed ID: 10196476 [TBL] [Abstract][Full Text] [Related]
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18. Pfeiffer syndrome caused by haploinsufficient mutation of FGFR2. Tsukuno M; Suzuki H; Eto Y J Craniofac Genet Dev Biol; 1999; 19(4):183-8. PubMed ID: 10731087 [TBL] [Abstract][Full Text] [Related]
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