Showing results (1601-1610 of 3,084) with videos related to
Sort By:
Pageof 309
Journal of Fish Diseases|June 17, 2011
Koi herpesvirus epizootic in cultured carp and koi, Cyprinus carpio L., in TaiwanL Cheng, C-Y Chen, M-A Tsai, et al.Taiwanese Journal of Obstetrics & Gynecology|January 4, 2012
Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumbChih-Ping Chen, Schu-Rern Chern, Chen-Yu Chen, et al.Taiwanese Journal of Obstetrics & Gynecology|February 19, 2022
Application of quantitative fluorescent polymerase chain reaction analysis for the rapid confirmation of trisomy 13 of maternal origin in a pregnancy with fetal holoprosencephaly, cyclopia, polydactyly, omphalocele and cell culture failureChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 20, 2022
Temporal Dynamics of Nasopharyngeal and Tracheal Severe Acute Respiratory Syndrome Coronavirus 2 Cycle Thresholds in Coronavirus Disease 2019 Patients With TracheostomySallie M Long, Alexander Chern, Victoria Cooley, et al.Mbio|October 12, 2021
A Novel Toxoplasma Inner Membrane Complex Suture-Associated Protein Regulates Suture Protein Targeting and Colocalizes with Membrane Trafficking MachineryJessica H Chern, Rebecca R Pasquarelli, Andy S Moon, et al.Taiwanese Journal of Obstetrics & Gynecology|April 1, 2022
Detection of paternal origin of fetal de novo rea(21q;21q) down syndrome in a pregnancy of a young woman associated with an abnormal first-trimester maternal serum screening resultChih-Ping Chen, Quan-Bin Jou, Schu-Rern Chern, et al.The Journal of Clinical Investigation|March 1, 1980
Linkage analysis between the major histocompatibility system and insulin-dependent diabetes in families with patients in two consecutive generationsJ Barbosa, M M Chern, V E Anderson, et al.European Journal of Medical Genetics|March 30, 2010
Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delayChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.Taiwanese Journal of Obstetrics & Gynecology|May 10, 2021
Prenatal diagnosis of trisomy 11 in a single colony of cultured amniocytes at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Cheng-En Hsieh, Schu-Rern Chern, et al.Taiwanese Journal of Obstetrics & Gynecology|July 17, 2012
Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcomeChih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.Pageof 309