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Case Report: Variations in the ALPL Gene in Chinese Patients With HypophosphatasiaQiang Zhang, Fei Shen, Zailong Qin et al.|Frontiers in Genetics|2021Cited by 6
[Analysis of genetic variants in four children with congenital hyperinsulinemia].Liang‐In Lin, Sheng He, Fei Shen et al.|PubMed|2021Cited by 3
Novel compound heterozygous variant of BSCL2 identified by whole exome sequencing and multiplex ligation‑dependent probe amplification in an infant with congenital generalized lipodystrophyBobo Xie, Yiping Shen, Jingsi Luo et al.|Molecular Medicine Reports|2020Cited by 1