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Chonglin Chen

Showing results (1-10 of 47) with videos related to

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Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|October 31, 2018
Persistent Fetal VasculatureChonglin Chen, Hu Xiao, Xiaoyan Ding
Frontiers in Medicine|July 17, 2023
Improvement in health-related quality of life with Botulinum toxin A injection in acquired superior oblique palsyChonglin Chen, Meiping Xu, Huanyun Yu, et al.
Genes|July 27, 2022
Clinical Features and Novel Genetic Variants Associated with Hermansky-Pudlak SyndromeChonglin Chen, Ruixin Wang, Yongguang Yuan, et al.
Retina (Philadelphia, Pa.)|September 22, 2025
Visual and Anatomic Outcomes of Vitrectomy for Myopic Maculoschisis with and without Macular Detachment: A Case-Control StudyJun Li, Chonglin Chen, Sufen Lu, et al.
Genes|May 27, 2026
Clinical Manifestations and Genetic Spectrum of Oculocutaneous Albinism Type 2 in Chinese PatientsChonglin Chen, Jun Li, Bingqi Wang, et al.
Experimental Eye Research|December 25, 2023
TYR mutation in a Chinese population with oculocutaneous albinism: Molecular characteristics and ophthalmic manifestationsChonglin Chen, Jun Li, Bingqi Wang, et al.
Applied Physics Letters|March 14, 2018
Role of temperature and oxygen content on structural and electrical properties of LaBaCo<sub>2</sub>O<sub>5+δ</sub> thin filmsBrennan Mace, Zach Harrell, Chonglin Chen, et al.
BMC Ophthalmology|December 14, 2020
New PTEN mutation identified in a patient with rare bilateral choroidal ganglioneuromaZhaoxin Jiang, Ting Zhang, Chonglin Chen, et al.
Ophthalmic Genetics|February 16, 2019
Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature reviewZhirong Wang, Limei Sun, Panfeng Wang, et al.
Journal of Ophthalmology|February 1, 2021
Novel Compound Heterozygous <i>BBS2</i> and Homozygous <i>MKKS</i> Variants Detected in Chinese Families with Bardet-Biedl SyndromeLi Huang, Limei Sun, Zhirong Wang, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|October 31, 2018
Persistent Fetal VasculatureChonglin Chen, Hu Xiao, Xiaoyan Ding
Frontiers in Medicine|July 17, 2023
Improvement in health-related quality of life with Botulinum toxin A injection in acquired superior oblique palsyChonglin Chen, Meiping Xu, Huanyun Yu, et al.
Genes|July 27, 2022
Clinical Features and Novel Genetic Variants Associated with Hermansky-Pudlak SyndromeChonglin Chen, Ruixin Wang, Yongguang Yuan, et al.
Retina (Philadelphia, Pa.)|September 22, 2025
Visual and Anatomic Outcomes of Vitrectomy for Myopic Maculoschisis with and without Macular Detachment: A Case-Control StudyJun Li, Chonglin Chen, Sufen Lu, et al.
Genes|May 27, 2026
Clinical Manifestations and Genetic Spectrum of Oculocutaneous Albinism Type 2 in Chinese PatientsChonglin Chen, Jun Li, Bingqi Wang, et al.
Experimental Eye Research|December 25, 2023
TYR mutation in a Chinese population with oculocutaneous albinism: Molecular characteristics and ophthalmic manifestationsChonglin Chen, Jun Li, Bingqi Wang, et al.
Applied Physics Letters|March 14, 2018
Role of temperature and oxygen content on structural and electrical properties of LaBaCo<sub>2</sub>O<sub>5+δ</sub> thin filmsBrennan Mace, Zach Harrell, Chonglin Chen, et al.
BMC Ophthalmology|December 14, 2020
New PTEN mutation identified in a patient with rare bilateral choroidal ganglioneuromaZhaoxin Jiang, Ting Zhang, Chonglin Chen, et al.
Ophthalmic Genetics|February 16, 2019
Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature reviewZhirong Wang, Limei Sun, Panfeng Wang, et al.
Journal of Ophthalmology|February 1, 2021
Novel Compound Heterozygous <i>BBS2</i> and Homozygous <i>MKKS</i> Variants Detected in Chinese Families with Bardet-Biedl SyndromeLi Huang, Limei Sun, Zhirong Wang, et al.
Pageof 5