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Lingqian Wu

Showing results (11-20 of 194) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|October 19, 2021
Novel variants in OSGEP leading to Galloway-Mowat syndrome by altering its subcellular localizationHua Teng, Chen Liang, Desheng Liang, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|August 28, 2015
[Analysis of the NDP gene in a Chinese family with X-linked recessive Norrie disease]Libin Mei, Yanru Huang, Qian Pan, et al.
Annals of Translational Medicine|February 23, 2023
The role of non-invasive prenatal testing and ultrasound in prenatal screening of fetal chromosomal abnormalities in singleton: a retrospective studyXiying Yuan, Wenjing Yong, Lei Dai, et al.
Molecular Vision|March 23, 2011
A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmusJunjie Hu, Desheng Liang, Jinjie Xue, et al.
Frontiers in Genetics|September 27, 2021
Simultaneous Identification of Both <i>MFSD8</i> and <i>RDH12</i> Pathogenic Variants in a Chinese Family Affected With Retinitis PigmentosaYihui Wang, Yanling Teng, Desheng Liang, et al.
Current Gene Therapy|August 10, 2020
Gene Therapy for Hemophilia A: Where We StandMiaojin Zhou, Zhiqing Hu, Chunhua Zhang, et al.
Journal of Child Neurology|June 26, 2014
Mutational analyses of the FMR1 gene in Chinese pediatric population of fragile x suspects: low tolerance for point mutationShiyu Luo, Wen Huang, Qiuping Xia, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 27, 2023
[Consensus on laboratory diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency]Yu Sun, Lingqian Wu, Lei Ye, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 4, 2011
Mutation analysis of the SRY, NR5A1, and DHH genes in six Chinese 46,XY womenXi Liao, Desheng Liang, Yanping Li, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 24, 2021
Increase in diagnostic yield achieved for 174 whole-exome sequencing cases reanalyzed 1-2 years after initial analysisYingdi Liu, Yanling Teng, Zhuo Li, et al.
Pageof 20

Showing results (11-20 of 194) with videos related to

Sort By:
Pageof 20
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 19, 2021
Novel variants in OSGEP leading to Galloway-Mowat syndrome by altering its subcellular localizationHua Teng, Chen Liang, Desheng Liang, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|August 28, 2015
[Analysis of the NDP gene in a Chinese family with X-linked recessive Norrie disease]Libin Mei, Yanru Huang, Qian Pan, et al.
Annals of Translational Medicine|February 23, 2023
The role of non-invasive prenatal testing and ultrasound in prenatal screening of fetal chromosomal abnormalities in singleton: a retrospective studyXiying Yuan, Wenjing Yong, Lei Dai, et al.
Molecular Vision|March 23, 2011
A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmusJunjie Hu, Desheng Liang, Jinjie Xue, et al.
Frontiers in Genetics|September 27, 2021
Simultaneous Identification of Both <i>MFSD8</i> and <i>RDH12</i> Pathogenic Variants in a Chinese Family Affected With Retinitis PigmentosaYihui Wang, Yanling Teng, Desheng Liang, et al.
Current Gene Therapy|August 10, 2020
Gene Therapy for Hemophilia A: Where We StandMiaojin Zhou, Zhiqing Hu, Chunhua Zhang, et al.
Journal of Child Neurology|June 26, 2014
Mutational analyses of the FMR1 gene in Chinese pediatric population of fragile x suspects: low tolerance for point mutationShiyu Luo, Wen Huang, Qiuping Xia, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 27, 2023
[Consensus on laboratory diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency]Yu Sun, Lingqian Wu, Lei Ye, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 4, 2011
Mutation analysis of the SRY, NR5A1, and DHH genes in six Chinese 46,XY womenXi Liao, Desheng Liang, Yanping Li, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 24, 2021
Increase in diagnostic yield achieved for 174 whole-exome sequencing cases reanalyzed 1-2 years after initial analysisYingdi Liu, Yanling Teng, Zhuo Li, et al.
Pageof 20