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Yong-jia Yang

Showing results (1-10 of 10) with videos related to

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[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|July 4, 2007
[A family of congenital fibrosis of extraocular muscles associated with juvenile canities]Jun Zhao, Kan-Xing Zhao, Ning-Dong Li, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Interstitial deletion 5q14.3q21.3 associated with lethal epilepsyYong-jia Yang, Xu Yao, Jihong Guo, et al.
American Journal of Medical Genetics. Part A|March 24, 2016
Trisomy 3 mosaicism in a 5-year-old boy with multiple anomalies: A very rare caseYong-Jia Yang, Xu Yao, Jihong Guo, et al.
Thescientificworldjournal|April 14, 2015
First report of CTNS mutations in a Chinese family with infantile cystinosisYong-jia Yang, Yuan Hu, Rui Zhao, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|July 29, 2003
[Exclusive gene mapping on retinitis pigmentosa with markers on chromosomes 3 in a Chinese kindred]Zheng Liu, Hao Deng, Xing-hua Xi, et al.
Biomed Research International|September 4, 2013
A novel splicing mutation of KIT results in piebaldism and auburn hair color in a Chinese familyYong-jia Yang, Rui Zhao, Xin-yu He, et al.
Journal of Ethnopharmacology|October 21, 2006
Subchronic toxicity studies of Radix Astragali extract in rats and dogsShu-Yi Yu, Hong-Tao Ouyang, Ju-Yun Yang, et al.
American Journal of Medical Genetics. Part A|January 21, 2014
SNAI2 mutation causes human piebaldismYong-jia Yang, Rui Zhao, Xin-yu He, et al.
Gene|January 29, 2013
First report of HGD mutations in a Chinese with alkaptonuriaYong-jia Yang, Ji-hong Guo, Wei-jian Chen, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 19, 2018
Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo MutationHong-Mei Zhao, Yong-Jia Yang, Jia-Qi Duan, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|July 4, 2007
[A family of congenital fibrosis of extraocular muscles associated with juvenile canities]Jun Zhao, Kan-Xing Zhao, Ning-Dong Li, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Interstitial deletion 5q14.3q21.3 associated with lethal epilepsyYong-jia Yang, Xu Yao, Jihong Guo, et al.
American Journal of Medical Genetics. Part A|March 24, 2016
Trisomy 3 mosaicism in a 5-year-old boy with multiple anomalies: A very rare caseYong-Jia Yang, Xu Yao, Jihong Guo, et al.
Thescientificworldjournal|April 14, 2015
First report of CTNS mutations in a Chinese family with infantile cystinosisYong-jia Yang, Yuan Hu, Rui Zhao, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|July 29, 2003
[Exclusive gene mapping on retinitis pigmentosa with markers on chromosomes 3 in a Chinese kindred]Zheng Liu, Hao Deng, Xing-hua Xi, et al.
Biomed Research International|September 4, 2013
A novel splicing mutation of KIT results in piebaldism and auburn hair color in a Chinese familyYong-jia Yang, Rui Zhao, Xin-yu He, et al.
Journal of Ethnopharmacology|October 21, 2006
Subchronic toxicity studies of Radix Astragali extract in rats and dogsShu-Yi Yu, Hong-Tao Ouyang, Ju-Yun Yang, et al.
American Journal of Medical Genetics. Part A|January 21, 2014
SNAI2 mutation causes human piebaldismYong-jia Yang, Rui Zhao, Xin-yu He, et al.
Gene|January 29, 2013
First report of HGD mutations in a Chinese with alkaptonuriaYong-jia Yang, Ji-hong Guo, Wei-jian Chen, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 19, 2018
Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo MutationHong-Mei Zhao, Yong-Jia Yang, Jia-Qi Duan, et al.
Pageof 1