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短肢畸形胎儿FGFR3基因突变分析

上传者:徐小白 |  格式:doc  |  页数:13 |  大小:38KB

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2016,428(20):3903-3910. Р [6] Del olo N,Sarabipour S,Hristova K. A New Method to Study Heterodimerization of Membrane Proteins and Its Application to Fibroblast Growth Factor Receptors [J]. J Biol Chem,2017,292(4):1288-1301. Р [7] Xue Y,Sun A,Mekikian PB,et al. FGFR3 mutation fre?鄄quency in 324 cases from the International Skeletal Dysplasia Registry [J]. Mol Genomic Med,2014,2(6):497-503. Р [8] Nagahara K,Harada Y,Futami T,et al. Japanese familial case of hypochondroplasia with a novel mutation in FGFR3 [J]. Clin Pediatr Endocrinol,2016,25(3):103-106. Р [9] Chen SW,Chen CP,Wang LK,et al. Perinatal imaging findings and molecular ic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G(p.Ter807Gly) (X807G) mutation in FGFR3 [J]. Taiwan J Obstet Gynecol,2017,56(1):87-92.

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