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Peikuan Cong

Showing results (1-10 of 9) with videos related to

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Parasitology International|September 12, 2009
Genomic organization and promoter analysis of the Trichomonas vaginalis core histone gene familiesPeikuan Cong, Yingfeng Luo, Weidong Bao, et al.
Scientific Reports|June 2, 2023
The causal mutation in ARR3 gene for high myopia and progressive color vision defectLei Gu, Peikuan Cong, Qingyao Ning, et al.
European Journal of Medical Genetics|February 2, 2013
A Chinese patient with KBG syndrome and a 9q31.2-33.1 microdeletionMingzhi Xu, Huali Zhou, Jing Yong, et al.
Gene|April 11, 2012
A large deletion/insertion-induced frameshift mutation of the androgen receptor gene in a family with a familial complete androgen insensitivity syndromePeikuan Cong, Yinghui Ye, Yue Wang, et al.
American Journal of Medical Genetics. Part A|July 8, 2010
Familial syndrome resembling Aarskog syndromeMingzhi Xu, Ming Qi, Huali Zhou, et al.
Human Mutation|September 3, 2010
LQTS gene LOVD databaseTao Zhang, Arthur Moss, Peikuan Cong, et al.
Human Mutation|September 9, 2011
Novel LOVD databases for hereditary breast cancer and colorectal cancer genes in the Chinese populationMin Pan, Peikuan Cong, Yue Wang, et al.
Nature Genetics|July 31, 2012
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosisPei-Wen Chiang, Juan Wang, Yang Chen, et al.
Human Mutation|July 10, 2019
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathiesLi Zhang, Qianqian Zhang, Yaohua Tang, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Parasitology International|September 12, 2009
Genomic organization and promoter analysis of the Trichomonas vaginalis core histone gene familiesPeikuan Cong, Yingfeng Luo, Weidong Bao, et al.
Scientific Reports|June 2, 2023
The causal mutation in ARR3 gene for high myopia and progressive color vision defectLei Gu, Peikuan Cong, Qingyao Ning, et al.
European Journal of Medical Genetics|February 2, 2013
A Chinese patient with KBG syndrome and a 9q31.2-33.1 microdeletionMingzhi Xu, Huali Zhou, Jing Yong, et al.
Gene|April 11, 2012
A large deletion/insertion-induced frameshift mutation of the androgen receptor gene in a family with a familial complete androgen insensitivity syndromePeikuan Cong, Yinghui Ye, Yue Wang, et al.
American Journal of Medical Genetics. Part A|July 8, 2010
Familial syndrome resembling Aarskog syndromeMingzhi Xu, Ming Qi, Huali Zhou, et al.
Human Mutation|September 3, 2010
LQTS gene LOVD databaseTao Zhang, Arthur Moss, Peikuan Cong, et al.
Human Mutation|September 9, 2011
Novel LOVD databases for hereditary breast cancer and colorectal cancer genes in the Chinese populationMin Pan, Peikuan Cong, Yue Wang, et al.
Nature Genetics|July 31, 2012
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosisPei-Wen Chiang, Juan Wang, Yang Chen, et al.
Human Mutation|July 10, 2019
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathiesLi Zhang, Qianqian Zhang, Yaohua Tang, et al.
Pageof 1