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Nurse Education in Practice|November 5, 2025
Effects of mobile learning applications for physical examination among nurse students: Use of the cardiovascular systemHui-Mei Chao, Shin-Wen Chen, Shu-Mei ChaoJournal of Medical Ultrasound|August 2, 2018
Prenatal Ultrasound Evaluation and Outcome of Pregnancy with Fetal Cystic Hygromas and LymphangiomasYen-Ni Chen, Chih-Ping Chen, Chen-Ju Lin, et al.Taiwanese Journal of Obstetrics & Gynecology|May 20, 2022
A false-positive result at non-invasive prenatal testing due to maternal 17p12 microduplicationChih-Ping Chen, Shin-Wen Chen, Peih-Shan Wu, et al.Taiwanese Journal of Obstetrics & Gynecology|September 10, 2022
The significance of karyotyping and azoospermia factor analysis in patients with nonobstructive azoospermia or oligozoospermiaShin-Wen Chen, Chih-Ping Chen, Schu-Rern Chern, et al.ACS Applied Materials & Interfaces|January 5, 2013
Self-assembled monolayer immobilized gold nanoparticles for plasmonic effects in small molecule organic photovoltaicMing-Chung Chen, Yi-Ling Yang, Shin-Wen Chen, et al.Taiwanese Journal of Obstetrics & Gynecology|February 11, 2020
Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosumChih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, et al.Taiwanese Journal of Obstetrics & Gynecology|March 8, 2021
Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL associationShih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, et al.Taiwanese Journal of Obstetrics & Gynecology|May 10, 2021
Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbsChih-Ping Chen, Shih-Shien Weng, Schu-Rern Chern, et al.Taiwanese Journal of Obstetrics & Gynecology|March 8, 2021
Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defectsChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.Taiwanese Journal of Obstetrics & Gynecology|January 26, 2021
Prenatal diagnosis of familial 2p15 microduplication associated with pulmonary artery stenosis, single umbilical artery and left foot postaxial polydactyly on fetal ultrasoundChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.Pageof 16