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Yunping Lei

Showing results (11-20 of 57) with videos related to

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Human Genetics|May 2, 2020
Somatic mutations in planar cell polarity genes in neural tissue from human fetuses with neural tube defectsTian Tian, Yunping Lei, Yongyan Chen, et al.
Iscience|May 11, 2023
Whole-exome sequencing study of hypospadiasZhongzhong Chen, Yunping Lei, Richard H Finnell, et al.
Plos One|August 8, 2013
Mutations in planar cell polarity gene SCRIB are associated with spina bifidaYunping Lei, Huiping Zhu, Cody Duhon, et al.
Journal of Human Genetics|September 5, 2008
Genetic imprint of the Mongol: signal from phylogeographic analysis of mitochondrial DNABaoweng Cheng, Wenru Tang, Li He, et al.
Human Mutation|December 30, 2014
Rare LRP6 variants identified in spina bifida patientsYunping Lei, Kristin Fathe, Danielle McCartney, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|September 26, 2023
A mutation in TBXT causes congenital vertebral malformations in humans and miceShuxia Chen, Yunping Lei, Yajun Yang, et al.
BMC Genomics|August 14, 2015
Analysis of archived residual newborn screening blood spots after whole genome amplificationBrandi L Cantarel, Yunping Lei, Daniel Weaver, et al.
BMC Medical Genomics|December 21, 2019
Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13Zhongzhong Chen, Xiaoling Lin, Yunping Lei, et al.
BMC Medical Genomics|April 6, 2018
Genetic analysis of Wnt/PCP genes in neural tube defectsZhongzhong Chen, Yunping Lei, Xuanye Cao, et al.
Biology|January 21, 2023
<i>KDM6B</i> Variants May Contribute to the Pathophysiology of Human Cerebral Folate DeficiencyXiao Han, Xuanye Cao, Robert M Cabrera, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Human Genetics|May 2, 2020
Somatic mutations in planar cell polarity genes in neural tissue from human fetuses with neural tube defectsTian Tian, Yunping Lei, Yongyan Chen, et al.
Iscience|May 11, 2023
Whole-exome sequencing study of hypospadiasZhongzhong Chen, Yunping Lei, Richard H Finnell, et al.
Plos One|August 8, 2013
Mutations in planar cell polarity gene SCRIB are associated with spina bifidaYunping Lei, Huiping Zhu, Cody Duhon, et al.
Journal of Human Genetics|September 5, 2008
Genetic imprint of the Mongol: signal from phylogeographic analysis of mitochondrial DNABaoweng Cheng, Wenru Tang, Li He, et al.
Human Mutation|December 30, 2014
Rare LRP6 variants identified in spina bifida patientsYunping Lei, Kristin Fathe, Danielle McCartney, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|September 26, 2023
A mutation in TBXT causes congenital vertebral malformations in humans and miceShuxia Chen, Yunping Lei, Yajun Yang, et al.
BMC Genomics|August 14, 2015
Analysis of archived residual newborn screening blood spots after whole genome amplificationBrandi L Cantarel, Yunping Lei, Daniel Weaver, et al.
BMC Medical Genomics|December 21, 2019
Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13Zhongzhong Chen, Xiaoling Lin, Yunping Lei, et al.
BMC Medical Genomics|April 6, 2018
Genetic analysis of Wnt/PCP genes in neural tube defectsZhongzhong Chen, Yunping Lei, Xuanye Cao, et al.
Biology|January 21, 2023
<i>KDM6B</i> Variants May Contribute to the Pathophysiology of Human Cerebral Folate DeficiencyXiao Han, Xuanye Cao, Robert M Cabrera, et al.
Pageof 6