Showing results (791-800 of 1,241) with videos related to

Sort By:
Pageof 125
Taiwanese Journal of Obstetrics & Gynecology|May 20, 2022
High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell lineChih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 31, 2024
Prenatal diagnosis of Jacobsen syndrome associated with a distal 11q deletion and a distal 8q duplication by chromosome microarray analysis in a fetus with a de novo unbalanced translocation of 46,XX,der(11)t(8;11)(q24.13;q23.3) and multiple congenital anomalies on fetal ultrasoundChih-Ping Chen, Jian-Pei Huang, Fang-Tzu Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 31, 2024
Prenatal diagnosis of a 14-Mb 11p11.2-p13 deletion by chromosome microarray analysis in a pregnancy with fetal recombinant chromosome 11 syndrome of rec(11)del(11)(p11.2p13)ins(11)(q21p11.2p13) and maternal intrachromosomal insertion of ins(11)(q21p11.2p13)Chih-Ping Chen, Chen-Yu Chen, Fang-Tzu Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 5, 2023
Mosaicism for Robertsonian jumping translocation at amniocentesis: 45,XY,der(15;22)(q10;q10)mat/46,XY,i(15)(q10)/46,XY, genetic counseling, prenatal diagnosis and postnatal follow-up in a pregnancy with a favorable fetal outcomeChih-Ping Chen, Jenn-Jhy Tseng, Fang-Tzu Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2019
Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasoundChih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, et al.
BMC Ophthalmology|January 1, 2020
Repeated intravitreal injections of antivascular endothelial growth factor in patients with neovascular age-related macular degeneration may increase the risk of ischemic optic neuropathyYu-Yen Chen, Pesus Chou, Yu-Fang Huang, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 11, 2020
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesisChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Science & Justice : Journal of the Forensic Science Society|January 16, 2018
Variation of δ<sup>2</sup>H, δ<sup>18</sup>O & δ<sup>13</sup>C in crude palm oil from different regions in Malaysia: Potential of stable isotope signatures as a key traceability parameterSyahidah Akmal Muhammad, Eng-Keng Seow, A K Mohd Omar, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 10, 2022
Progressive increase of the mosaic level for 45,X in 45,X/46, XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46, XX fetus with a favorable outcomeChih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, et al.
Frontiers in Genetics|March 6, 2023
The impact of alcoholic drinks and dietary factors on epigenetic markers associated with triglyceride levelsChao-Qiang Lai, Laurence D Parnell, Yu-Chi Lee, et al.
Pageof 125