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Gene|July 16, 2013
Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytesChih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, et al.Nature Methods|July 6, 2021
PaintSHOP enables the interactive design of transcriptome- and genome-scale oligonucleotide FISH experimentsElliot A Hershberg, Conor K Camplisson, Jennie L Close, et al.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|September 23, 2019
Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defectsChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.Human Molecular Genetics|January 11, 2017
Targeting ENT1 and adenosine tone for the treatment of Huntington's diseaseYu-Han Kao, Meng-Syuan Lin, Chiung-Mei Chen, et al.Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delayChih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, et al.Neurosurgery|February 8, 2022
Revascularization Is Associated With a Reduced Stroke Risk in Patients With Sickle Cell-Associated Moyamoya SyndromeSarah Newman, J Tanner McMahon, Jason H Boulter, et al.Cardiology in the Young|November 15, 2023
Perception towards palliative care among patients with pulmonary hypertension in malaysia: a correlation with disease statusSue Kiat Tye, Norazlina Susila Razali, Shakila Amira Ahmad Shauqi, 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|January 26, 2021
Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphismChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.Pageof 309