Genotype-Phenotype Correlation Analysis of WT1 Gene Variants in Denys-Drash Syndrome and Frasier Syndrome by CAO Yaqing, GUO Baocheng, NIE Min

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Application status of risk assessment models for periodontal disease by NIE Min, XU Hongdan, WU Yafei, YANG Jingmei

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Correlation between different FGFR1 mutations and congenital hypogonadotropic hypogonadism by YANG Yufan, WANG Xi, NIE Min, WU Xueyan, MAO Jiangfeng

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Sex hormone replacement therapy for patients with Prader-Willi syndrome by WANG Liang, WANG Xi, NIE Min, WU Xueyan, MAO Jiangfeng

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Prevention and Control of Waste Plastics Pollution in China by Wang Qi, Qu Jinping, Shi Bi, Chen Ning, Nie Min, Yang Shuangqiao

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A case of Kabuki syndrome with precocious puberty and short stature due to novel KDM6A splice-site mutation by ZHAO Ya-ling, LI Shu-ying, WANG Xi, NIE Min, WU Xue-yan, MAO Jiang-feng

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A case of micropenis caused by compound heterozygote mutations in luteinizing hormone/choriogonadotropin receptor (LHCGR) by YANG Yu-fan, ZHAO Ya-ling, WANG Xi, NIE Min, WU Xue-yan, MAO Jiang-feng

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