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Taiwanese Journal of Obstetrics & Gynecology|January 5, 2010
Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesisChih-Ping Chen, Schu-Rern Chern, Pei-Chen Wu, et al.Plos One|December 22, 2018
Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populationsJargalkhuu Erdenechuluun, Yin-Hung Lin, Khongorzul Ganbat, et al.Journal of Personalized Medicine|February 25, 2023
Etiological Diagnosis and Personalized Therapy for Hypertension: A Hypothesis of the REASOH ClassificationChong Xu, Moran Li, Weilun Meng, et al.Taiwanese Journal of Obstetrics & Gynecology|February 21, 2018
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalitiesChih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, et al.Diagnostics (Basel, Switzerland)|December 24, 2021
Preimplantation Genetic Diagnosis in Hereditary Hearing ImpairmentHsin-Lin Chen, Pei-Hsuan Lin, Yu-Ting Chiang, et al.Free Radical Biology & Medicine|December 25, 2025
Ginkgolic acid ameliorates pressure overload-induced cardiac remodeling by inhibiting SAE1 and activating the NRF2/HMOX1 pathwayXuening Dang, Qingqi Ji, Zhenyu Huang, et al.Journal of Neurochemistry|April 15, 2025
Liver Diseases and Brain Disorders: Genetic Mechanisms and Biomarker Pathways in a Prospective Cohort Study From the UK BiobankHai-Hua Guo, Pei-Yang Gao, Wei Zhang, et al.Taiwanese Journal of Obstetrics & Gynecology|October 19, 2016
Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversionChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.Taiwanese Journal of Obstetrics & Gynecology|August 17, 2010
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, et al.Taiwanese Journal of Obstetrics & Gynecology|November 9, 2010
Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridizationChih-Ping Chen, Yung-Ting Kuo, Shuan-Pei Lin, et al.Pageof 62