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Lingqian Wu

Showing results (1-10 of 194) with videos related to

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BMC Pediatrics|February 18, 2018
Clinical and genetic study of 20 patients from China with Cornelia de Lange syndromeMingyan Hei, Xiangyu Gao, Lingqian Wu
Gene|May 22, 2019
Identification of six novel mutations in five infants with suspected maple syrup urine disease based on blood and urine metabolism screeningChenxi Yang, Siyuan Linpeng, Yingxi Cao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 17, 2016
[Influence of chromosomal polymorphisms on the clinical outcome of patients undergoing in vitro fertilization embryo transfer]Yumei Li, Donge Liu, Zhongyuan Yao, et al.
Human Gene Therapy|January 26, 2018
Gene Therapy for Hemophilia and Duchenne Muscular Dystrophy in ChinaXionghao Liu, Mujun Liu, Lingqian Wu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2019
[A case of Antley-Bixler syndrome caused by novel POR mutations]Can Peng, Chengzi Huang, Hu Tan, et al.
Orphanet Journal of Rare Diseases|February 17, 2019
Next generation sequencing identified two novel mutations in NIPBL and a frame shift mutation in CREBBP in three Chinese childrenHui Tang, Jing Guo, Siyuan Linpeng, et al.
Journal of Clinical Laboratory Analysis|September 27, 2019
Development and validation of a haplotype-free technique for non-invasive prenatal diagnosis of spinal muscular atrophyXianda Wei, Weigang Lv, Hu Tan, et al.
Gene|December 3, 2014
Two novel NIPBL gene mutations in Chinese patients with Cornelia de Lange syndromeLibin Mei, Desheng Liang, Yanru Huang, et al.
Genetic Testing and Molecular Biomarkers|August 4, 2012
Mutation analysis in Chinese patients with Cornelia de Lange syndromeQiulian Zhong, Desheng Liang, Jing Liu, et al.
Frontiers in Genetics|October 11, 2021
Prenatal Diagnosis in a Fetus With X-Linked Recessive Chondrodysplasia Punctata: Identification and Functional Study of a Novel Missense Mutation in <i>ARSE</i>Li Zhang, Haoran Hu, Desheng Liang, et al.
Pageof 20

Showing results (1-10 of 194) with videos related to

Sort By:
Pageof 20
BMC Pediatrics|February 18, 2018
Clinical and genetic study of 20 patients from China with Cornelia de Lange syndromeMingyan Hei, Xiangyu Gao, Lingqian Wu
Gene|May 22, 2019
Identification of six novel mutations in five infants with suspected maple syrup urine disease based on blood and urine metabolism screeningChenxi Yang, Siyuan Linpeng, Yingxi Cao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 17, 2016
[Influence of chromosomal polymorphisms on the clinical outcome of patients undergoing in vitro fertilization embryo transfer]Yumei Li, Donge Liu, Zhongyuan Yao, et al.
Human Gene Therapy|January 26, 2018
Gene Therapy for Hemophilia and Duchenne Muscular Dystrophy in ChinaXionghao Liu, Mujun Liu, Lingqian Wu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2019
[A case of Antley-Bixler syndrome caused by novel POR mutations]Can Peng, Chengzi Huang, Hu Tan, et al.
Orphanet Journal of Rare Diseases|February 17, 2019
Next generation sequencing identified two novel mutations in NIPBL and a frame shift mutation in CREBBP in three Chinese childrenHui Tang, Jing Guo, Siyuan Linpeng, et al.
Journal of Clinical Laboratory Analysis|September 27, 2019
Development and validation of a haplotype-free technique for non-invasive prenatal diagnosis of spinal muscular atrophyXianda Wei, Weigang Lv, Hu Tan, et al.
Gene|December 3, 2014
Two novel NIPBL gene mutations in Chinese patients with Cornelia de Lange syndromeLibin Mei, Desheng Liang, Yanru Huang, et al.
Genetic Testing and Molecular Biomarkers|August 4, 2012
Mutation analysis in Chinese patients with Cornelia de Lange syndromeQiulian Zhong, Desheng Liang, Jing Liu, et al.
Frontiers in Genetics|October 11, 2021
Prenatal Diagnosis in a Fetus With X-Linked Recessive Chondrodysplasia Punctata: Identification and Functional Study of a Novel Missense Mutation in <i>ARSE</i>Li Zhang, Haoran Hu, Desheng Liang, et al.
Pageof 20