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1. A start codon mutation of the TSPAN12 gene in Chinese families causes clinical heterogeneous familial exudative vitreoretinopathy. Issue 10 (26th August 2019)

5. Comprehensive evaluation of BRCA1/2 variant interpretation ability among laboratories in China. Issue 3 (4th January 2021)

8. Exome sequencing of Saudi Arabian patients with ADPKD. (1st January 2019)