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Yapeng Zhou

Showing results (11-20 of 17) with videos related to

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Molecular Genetics & Genomic Medicine|January 19, 2023
Clinical features and molecular characterization of Chinese patients with FKBP10 variantsZhijia Tan, Hiu Tung Shek, Peikai Chen, et al.
Clinical Genetics|November 20, 2025
Expanding the Genotype and Phenotype Diversity in a Chinese Cohort With TRPV4-Related DysplasiaLina Dong, Kwan Chun Ho, Zhijia Tan, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 1, 2022
Retrospective analyses of clinical features in 28 Chinese patients with type V osteogenesis imperfecta: new perspectives in an old issueZhijia Tan, Hiu Tung Shek, Zhongxin Dong, et al.
Frontiers in Genetics|February 14, 2022
Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I CollagenPeikai Chen, Zhijia Tan, Hiu Tung Shek, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 10, 2024
Multi-omics analyses reveal aberrant differentiation trajectory with WNT1 loss-of-function in type XV osteogenesis imperfectaZhijia Tan, Peikai Chen, Jianan Zhang, et al.
Orphanet Journal of Rare Diseases|September 20, 2023
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patientsPeikai Chen, Yapeng Zhou, Zhijia Tan, et al.
Orphanet Journal of Rare Diseases|June 28, 2022
Patient-reported outcomes in a Chinese cohort of osteogenesis imperfecta unveil psycho-physical stratifications associated with clinical manifestationsPeikai Chen, Zhijia Tan, Anmei Qiu, et al.
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Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Molecular Genetics & Genomic Medicine|January 19, 2023
Clinical features and molecular characterization of Chinese patients with FKBP10 variantsZhijia Tan, Hiu Tung Shek, Peikai Chen, et al.
Clinical Genetics|November 20, 2025
Expanding the Genotype and Phenotype Diversity in a Chinese Cohort With TRPV4-Related DysplasiaLina Dong, Kwan Chun Ho, Zhijia Tan, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 1, 2022
Retrospective analyses of clinical features in 28 Chinese patients with type V osteogenesis imperfecta: new perspectives in an old issueZhijia Tan, Hiu Tung Shek, Zhongxin Dong, et al.
Frontiers in Genetics|February 14, 2022
Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I CollagenPeikai Chen, Zhijia Tan, Hiu Tung Shek, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 10, 2024
Multi-omics analyses reveal aberrant differentiation trajectory with WNT1 loss-of-function in type XV osteogenesis imperfectaZhijia Tan, Peikai Chen, Jianan Zhang, et al.
Orphanet Journal of Rare Diseases|September 20, 2023
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patientsPeikai Chen, Yapeng Zhou, Zhijia Tan, et al.
Orphanet Journal of Rare Diseases|June 28, 2022
Patient-reported outcomes in a Chinese cohort of osteogenesis imperfecta unveil psycho-physical stratifications associated with clinical manifestationsPeikai Chen, Zhijia Tan, Anmei Qiu, et al.
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