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Sen Zhao

Showing results (341-350 of 346) with videos related to

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NPJ Genomic Medicine|December 8, 2021
De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalitiesVolkan Okur, Zefu Chen, Liesbeth Vossaert, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 2024
Core planar cell polarity genes <i>VANGL1</i> and <i>VANGL2</i> in predisposition to congenital vertebral malformationsXin Feng, Yongyu Ye, Jianan Zhang, et al.
American Journal of Human Genetics|January 12, 2021
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndromeNa Chen, Sen Zhao, Angad Jolly, et al.
Journal of Medical Genetics|May 9, 2020
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)Sen Zhao, Yuanqiang Zhang, Weisheng Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2019
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage modelJiaqi Liu, Nan Wu, , et al.
Biomedical and Environmental Sciences : BES|January 21, 2021
Association of Overlapped and Un-overlapped Comorbidities with COVID-19 Severity and Treatment Outcomes: A Retrospective Cohort Study from Nine Provinces in ChinaYan Ma, Dong Shan Zhu, Ren Bo Chen, et al.
Pageof 35

Showing results (341-350 of 346) with videos related to

Sort By:
Pageof 35
You have reached the last page of results.This site can display upto 346 results.
NPJ Genomic Medicine|December 8, 2021
De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalitiesVolkan Okur, Zefu Chen, Liesbeth Vossaert, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 2024
Core planar cell polarity genes <i>VANGL1</i> and <i>VANGL2</i> in predisposition to congenital vertebral malformationsXin Feng, Yongyu Ye, Jianan Zhang, et al.
American Journal of Human Genetics|January 12, 2021
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndromeNa Chen, Sen Zhao, Angad Jolly, et al.
Journal of Medical Genetics|May 9, 2020
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)Sen Zhao, Yuanqiang Zhang, Weisheng Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2019
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage modelJiaqi Liu, Nan Wu, , et al.
Biomedical and Environmental Sciences : BES|January 21, 2021
Association of Overlapped and Un-overlapped Comorbidities with COVID-19 Severity and Treatment Outcomes: A Retrospective Cohort Study from Nine Provinces in ChinaYan Ma, Dong Shan Zhu, Ren Bo Chen, et al.
Pageof 35