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Wang L, Wang X, He B, Cai N, Li W, Lou C, Xin S, Wu Q, Yu W, Qiang R. Mutation analysis of the phenylalanine hydroxylase gene and prenatal diagnosis of phenylketonuria in Shaanxi, China. J Pediatr Endocrinol Metab. 2017;30:1305-1310. Abstract

Wang L, Wang X, Cai X, Qiang R. Study of mitochondrial DNA A1555G and C1494T mutations in a large cohort of women individuals. Mitochondrial DNA A DNA Mapp Seq Anal. 2018:1-4. Abstract