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Peining Li

Showing results (21-30 of 130) with videos related to

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BMJ Case Reports|February 27, 2013
Absence of aneuploidy and gastrointestinal tumours in a man with a chromosomal 2q13 deletion and BUB1 monoallelic deficiencyDon Hoang, Gloria R Sue, Fang Xu, et al.
Case Reports in Genetics|November 8, 2012
Prenatal diagnosis and postnatal followup of partial trisomy 13q and partial monosomy 10p: a case report and review of the literatureYuan Wei, Xuefeng Gao, Liying Yan, et al.
American Journal of Infection Control|May 29, 2020
The impact of novel coronavirus SARS-CoV-2 among healthcare workers in hospitals: An aerial overviewBoqi Xiang, Peining Li, Xinhui Yang, et al.
Cancer Genetics and Cytogenetics|May 28, 2008
Double-minute MYC amplification and deletion of MTAP, CDKN2A, CDKN2B, and ELAVL2 in an acute myeloid leukemia characterized by oligonucleotide-array comparative genomic hybridizationAnitha Kamath, Harold Tara, Bixia Xiang, et al.
Optics Letters|February 15, 2024
Optical nanoimaging of laser-switched phase-change plasmonic infrared antennasQiyu Chen, Dunzhu Lu, Tianwei Qin, et al.
Case Reports in Genetics|April 22, 2022
Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated LiposarcomaHongyan Chai, Fang Xu, Autumn DiAdamo, et al.
Molecular Cytogenetics|December 23, 2014
Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalitiesZhiyong Xu, Qian Geng, Fuwei Luo, et al.
Fetal and Pediatric Pathology|December 6, 2017
Prenatal Diagnosis of Twin Fetuses with a Novel AR Gene Mutation in a Chinese Family of Complete Androgen Insensitivity SyndromeWeiqing Wu, Qian Geng, Yang Liu, et al.
Molecular Cytogenetics|December 23, 2017
De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndromeQin Wang, Qian Geng, Qinghua Zhou, et al.
Optics Express|November 3, 2017
Exploring the detection limits of infrared near-field microscopy regarding small buried structures and pushing them by exploiting superlens-related effectsLena Jung, Benedikt Hauer, Peining Li, et al.
Pageof 13

Showing results (21-30 of 130) with videos related to

Sort By:
Pageof 13
BMJ Case Reports|February 27, 2013
Absence of aneuploidy and gastrointestinal tumours in a man with a chromosomal 2q13 deletion and BUB1 monoallelic deficiencyDon Hoang, Gloria R Sue, Fang Xu, et al.
Case Reports in Genetics|November 8, 2012
Prenatal diagnosis and postnatal followup of partial trisomy 13q and partial monosomy 10p: a case report and review of the literatureYuan Wei, Xuefeng Gao, Liying Yan, et al.
American Journal of Infection Control|May 29, 2020
The impact of novel coronavirus SARS-CoV-2 among healthcare workers in hospitals: An aerial overviewBoqi Xiang, Peining Li, Xinhui Yang, et al.
Cancer Genetics and Cytogenetics|May 28, 2008
Double-minute MYC amplification and deletion of MTAP, CDKN2A, CDKN2B, and ELAVL2 in an acute myeloid leukemia characterized by oligonucleotide-array comparative genomic hybridizationAnitha Kamath, Harold Tara, Bixia Xiang, et al.
Optics Letters|February 15, 2024
Optical nanoimaging of laser-switched phase-change plasmonic infrared antennasQiyu Chen, Dunzhu Lu, Tianwei Qin, et al.
Case Reports in Genetics|April 22, 2022
Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated LiposarcomaHongyan Chai, Fang Xu, Autumn DiAdamo, et al.
Molecular Cytogenetics|December 23, 2014
Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalitiesZhiyong Xu, Qian Geng, Fuwei Luo, et al.
Fetal and Pediatric Pathology|December 6, 2017
Prenatal Diagnosis of Twin Fetuses with a Novel AR Gene Mutation in a Chinese Family of Complete Androgen Insensitivity SyndromeWeiqing Wu, Qian Geng, Yang Liu, et al.
Molecular Cytogenetics|December 23, 2017
De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndromeQin Wang, Qian Geng, Qinghua Zhou, et al.
Optics Express|November 3, 2017
Exploring the detection limits of infrared near-field microscopy regarding small buried structures and pushing them by exploiting superlens-related effectsLena Jung, Benedikt Hauer, Peining Li, et al.
Pageof 13