1. Targeted next‑generation sequencing identifies two novel COL2A1 gene mutations in Stickler syndrome with bilateral retinal detachment
   Xinhua Huang et al, 2018, International Journal of Molecular Medicine CrossRef
2. Genetic variations in Bestrophin‑1 and associated clinical findings in two Chinese patients with juvenile‑onset and adult‑onset best vitelliform macular dystrophy
   Ying Lin et al, 2017, Molecular Medicine Reports CrossRef
3. Novel Compound Heterozygous Variations in MPDZ Gene Caused Isolated Bilateral Macular Coloboma in a Chinese Family
   Shuang Zhang et al, 2022, Cells CrossRef
4. A Systematic Review of the Clinical Manifestations and Diagnostic Methods for Macular Coloboma
   Xiaoyi Hou et al, 2021, Current Eye Research CrossRef
5. A boy with amblyopia and familial exudative vitreoretinopathy harboring a new mutation of LRP5 and OPA1: A case report
   Chunli Chen et al, 2022, Frontiers in Genetics CrossRef
6. Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy
   Ying Lin et al, 2017, International Journal of Molecular Medicine CrossRef
7. Bilateral congenital macular coloboma and cataract
   Canwei Zhang et al, 2019, Medicine CrossRef