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Genetics and Molecular Research : GMR|June 21, 2016
IL-16 rs4778889 polymorphism contribution to the development of renal cell cancer in a Chinese populationS X Yang, F Chen, J W Zhang, et al.Prenatal Diagnosis|June 11, 1998
Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bonesC P Chen, S R Chern, C C Lee, et al.Prenatal Diagnosis|January 13, 1999
Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, urinary tract anomalies, congenital heart defect and kyphoscoliosisC P Chen, C C Lee, C W Pan, et al.Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis of a fetus with distal 10q trisomyC P Chen, J C Shih, C C Lee, et al.Prenatal Diagnosis|October 4, 2000
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18C P Chen, S R Chern, L F Yeh, et al.Prenatal Diagnosis|April 1, 1997
Prenatal diagnosis of cephalothoracopagus janiceps monosymmetrosC P Chen, C C Lee, F F Liu, et al.The British Journal of Surgery|April 12, 2006
Long-term outcome of resection of large hepatocellular carcinomaX-P Chen, F-Z Qiu, Z-D Wu, et al.Prenatal Diagnosis|May 29, 1998
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetusC P Chen, S R Chern, C C Lee, et al.Journal of Chromatography. B, Biomedical Sciences and Applications|July 20, 1999
Measurement of unbound caffeic acid in rat blood by on-line microdialysis coupled with liquid chromatography and its application to pharmacokinetic studyT H Tsai, Y F Chen, I F Chen, et al.Prenatal Diagnosis|October 4, 2000
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXYC P Chen, S R Chern, C L Chang, et al.Pageof 979