Showing results (2011-2020 of 3,091) with videos related to

Sort By:
Pageof 310
Taiwanese Journal of Obstetrics & Gynecology|November 19, 2021
Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndromeChih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorderChih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2022
Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 2q12.2→q13 encompassing MALL, NPHP1, RGPD6 and BUB1Chih-Ping Chen, Shin-Wen Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2022
Rapid confirmation of trisomy 13 of maternal origin by QF-PCR following postmortem tissue cell culture failure in a pregnancy with trisomy 13 at amniocentesis and fetal postaxial polydactyly and facial cleftChih-Ping Chen, Shin-Wen Chen, Jain-Pei Huang, et al.
Neurobiology of Disease|January 20, 2023
Deletion of equilibrative nucleoside transporter 2 disturbs energy metabolism and exacerbates disease progression in an experimental model of Huntington's diseaseChing-Ya Chen, Fang-Yi Chou, Ya-Gin Chang, et al.
Heliyon|January 7, 2021
Determinants of 3Rs behaviour in plastic usage: A study among MalaysiansLoh Chun T'ing, Krishna Moorthy, Chin Yoon Mei, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 12, 2021
Prenatal diagnosis of recurrent mosaic ring chromosome 13 of maternal originChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Prenatal Diagnosis|May 16, 2003
Prenatal diagnosis of de novo terminal deletion of chromosome 7qChih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|September 1, 1992
Microencapsulated pancreatic islets: a pathologic studyF J Leu, C F Chen, W E Chiang, et al.
Prenatal Diagnosis|February 14, 2006
Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangementsChih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, et al.
Pageof 310