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See Latest ArticlesFGFR3 Gene Mutations in Chinese Cases of Thanatophoric Dysplasia Type 1
Fetal Diagnosis and Therapy, 10/21/09
Yang Y et al. – The results suggest that the R248C mutation may serve as the primarily targeted one of the FGFR3 gene for rapid molecular diagnosis of TD 1.
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Continuous infusion of 17-hydroxyprogesterone caproate into either the fetoplacental or intervillous circulation of a placental cotyledon attenuates vasoconstriction of the fetoplacental arteries by thromboxane mimetic U46619
American Journal of Obstetrics and Gynecology, 12/17/09
The Influence of Phototherapy on Serum Cytokine Concentrations in Newborn Infants
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