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Genetic Counseling (Geneva, Switzerland)|October 28, 2011
A 24.2-Mb deletion of 4q12 --> q21.21 characterized by array CGH in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed pubertyC P Chen, S P Lin, Y N Su, et al.Taiwanese Journal of Obstetrics & Gynecology|February 19, 2022
Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcomeChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.Frontiers in Psychology|October 25, 2021
"We Are All Trying to Find a Way to Help Ourselves": A Look at Self-Help Strategies Among Psychotherapy ClientsSherilyn Chang, Rajeswari Sambasivam, Esmond Seow, et al.Journal of the International AIDS Society|March 24, 2022
Towards the first 90: impact of the national HIV self-test program on case finding and factors associated with linkage to confirmatory diagnosis in TaiwanYen-Fang Huang, Yu-Ching Huang, Yi-Chun Lo, et al.Journal of Neurochemistry|June 1, 1999
Modulation of dopamine transporter activity by nicotinic acetylcholine receptors and membrane depolarization in rat pheochromocytoma PC12 cellsC L Huang, H C Chen, N K Huang, et al.Taiwanese Journal of Obstetrics & Gynecology|May 18, 2020
Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcomeChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.Human Molecular Genetics|April 5, 2014
Inhibition of soluble tumor necrosis factor is therapeutic in Huntington's diseaseHan-Yun Hsiao, Feng-Lan Chiu, Chiung-Mei Chen, et al.Taiwanese Journal of Obstetrics & Gynecology|January 2, 2017
Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormalityChih-Ping Chen, Chung-Hu Fu, Yi-Hui Lin, et al.Taiwanese Journal of Obstetrics & Gynecology|September 10, 2022
Detection of mosaicism for 46,X,i(Y) (q10) in the blood lymphocytes in a phenotypically normal male neonate with prenatally detected 45,X/46, XY at amniocentesis and cytogenetic discrepancy in various tissuesChih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, et al.Taiwanese Journal of Obstetrics & Gynecology|April 30, 2016
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)Chih-Ping Chen, Fung-Yu Hung, Schu-Rern Chern, et al.Pageof 309