Chonglin Chen

发表

Symmetry of folds in FEVR: A genotype-phenotype correlation study.

Zhirong Wang, Chonglin Chen, Limei Sun, 2019, Experimental eye research.

ASSESSING THE ACTIVITY OF MYOPIC CHOROIDAL NEOVASCULARIZATION

Zhirong Wang, Chonglin Chen, Limei Sun, 2019, Retina.

The developmental changes of retinal microvasculature in children: a quantitative analysis using OCT angiography.

Zhirong Wang, Chonglin Chen, Limei Sun, 2020, American journal of ophthalmology.

Novel Compound Heterozygous BBS2 and Homozygous MKKS Variants Detected in Chinese Families with Bardet–Biedl Syndrome

Zhirong Wang, Chonglin Chen, Limei Sun, 2021, Journal of ophthalmology.

New PTEN mutation identified in a patient with rare bilateral choroidal ganglioneuroma

Ting Zhang, Chonglin Chen, Limei Sun, 2020, BMC Ophthalmology.

New mutation in PTEN identified in patient with rare bilateral choroidal ganglioneuroma

Ting Zhang, Chonglin Chen, Limei Sun, 2020 .

Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature review

Weiqing Wang, Panfeng Wang, Zhirong Wang, 2019, Ophthalmic genetics.

Persistent Fetal Vasculature

Chonglin Chen, Xiaoyan Ding, Hu Xiao, 2019, Asia-Pacific journal of ophthalmology.

Mutation Spectrum and De Novo Mutation Analysis in Stickler Syndrome Patients with High Myopia or Retinal Detachment

Ting Zhang, Zhirong Wang, Chonglin Chen, 2020, Genes.

Clinical features of ocular toxocariasis: a comparison between ultra-wide-field and conventional camera imaging

Chengxi Liu, Weiqing Wang, Ting Zhang, 2020, Eye.

Ultra-wide-field scanning laser ophthalmoscopy and optical coherence tomography in FEVR: findings and its diagnostic ability

Ting Zhang, Zhirong Wang, Chonglin Chen, 2020, British Journal of Ophthalmology.

Analysis of Etiologic Factors in Pediatric Rhegmatogenous Retinal Detachment with Genetic Testing.

Zhirong Wang, Chonglin Chen, Limei Sun, 2020, American journal of ophthalmology.

The spectrum of genetic mutations in patients with asymptomatic mild familial exudative vitreoretinopathy.

Ting Zhang, Zhirong Wang, Chonglin Chen, 2020, Experimental eye research.

Clinical manifestation and genetic analysis in Chinese early onset X‐linked retinoschisis

Wenmin Sun, Panfeng Wang, Zhirong Wang, 2020, Molecular genetics & genomic medicine.

Optical Coherence Tomography Angiography in Familial Exudative Vitreoretinopathy: Clinical Features and Phenotype-Genotype Correlation.

Zhirong Wang, Chonglin Chen, Limei Sun, 2018, Investigative ophthalmology & visual science.

Novel variants in familial exudative vitreoretinopathy patients with KIF11 mutations and the Genotype-Phenotype correlation.

Ting Zhang, Zhirong Wang, Chonglin Chen, 2020, Experimental eye research.

Clinical Features and Novel Genetic Variants Associated with Hermansky-Pudlak Syndrome

Ruixin Wang, Chonglin Chen, Yongguang Yuan, 2022, Genes.

Reading speed in school-age children with intermittent exotropia

Chonglin Chen, J. Bao, Xinping Yu, 2022, Scientific Reports.

Next-Generation Sequencing in the Familial Exudative Vitreoretinopathy-Associated Rhegmatogenous Retinal Detachment.

Zhirong Wang, Chonglin Chen, Limei Sun, 2019, Investigative ophthalmology & visual science.

Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease

Ting Zhang, Zhirong Wang, Chonglin Chen, 2020, Genes.

Retina Next-Generation Sequencing in the Familial Exudative Vitreoretinopathy-Associated Rhegmatogenous Retinal Detachment

Xiaoling, Zhirong Wang, Chonglin Chen, 2019 .