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Yu-Peng Liu

Showing results (121-130 of 187) with videos related to

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Gene|August 13, 2013
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsyChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
European Journal of Medical Genetics|July 31, 2012
A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndromeChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 14, 2015
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic herniaChih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|January 20, 2016
[Psychomotor retardation and intermitent convulsions for 8 months in an infant]Yuan Ding, Xi-Yuan Li, Yu-Peng Liu, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 28, 2011
Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findingsChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
Veterinary Microbiology|May 7, 2013
Genetic variation and phylogenetic analysis of hemagglutinin genes of H9 avian influenza viruses isolated in China during 2010-2012Rui-ai Chen, Han-zhang Lai, Lin Li, et al.
Gene|April 13, 2013
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delayChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
Andrology|December 31, 2024
CENP-E haploinsufficiency causes chromosome misalignment and spindle assembly checkpoint activation in the spermatogoniaJie Chen, Jie-Jie He, Shan Wu, et al.
The Kaohsiung Journal of Medical Sciences|October 9, 2024
Higher skin sympathetic nerve activity as a potential predictor of overactive bladder in females refractory to oral monotherapyYu-Chen Chen, Hao-Wei Chen, Tien-Chi Huang, et al.
Digestive Diseases and Sciences|June 22, 2026
Integrative Transcriptomic and Proteomic Profiling Identifies S100P as a Potential Functional Biomarker for Sessile Serrated LesionsJen-Hao Yeh, Chia-Chi Chen, Chih-I Chen, et al.
Pageof 19

Showing results (121-130 of 187) with videos related to

Sort By:
Pageof 19
Gene|August 13, 2013
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsyChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
European Journal of Medical Genetics|July 31, 2012
A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndromeChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 14, 2015
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic herniaChih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|January 20, 2016
[Psychomotor retardation and intermitent convulsions for 8 months in an infant]Yuan Ding, Xi-Yuan Li, Yu-Peng Liu, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 28, 2011
Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findingsChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
Veterinary Microbiology|May 7, 2013
Genetic variation and phylogenetic analysis of hemagglutinin genes of H9 avian influenza viruses isolated in China during 2010-2012Rui-ai Chen, Han-zhang Lai, Lin Li, et al.
Gene|April 13, 2013
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delayChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
Andrology|December 31, 2024
CENP-E haploinsufficiency causes chromosome misalignment and spindle assembly checkpoint activation in the spermatogoniaJie Chen, Jie-Jie He, Shan Wu, et al.
The Kaohsiung Journal of Medical Sciences|October 9, 2024
Higher skin sympathetic nerve activity as a potential predictor of overactive bladder in females refractory to oral monotherapyYu-Chen Chen, Hao-Wei Chen, Tien-Chi Huang, et al.
Digestive Diseases and Sciences|June 22, 2026
Integrative Transcriptomic and Proteomic Profiling Identifies S100P as a Potential Functional Biomarker for Sessile Serrated LesionsJen-Hao Yeh, Chia-Chi Chen, Chih-I Chen, et al.
Pageof 19