Xiao-lan Gao

Spectrum Analysis of Common Inherited Metabolic Diseases in Chinese Patients Screened and Diagnosed by Tandem Mass Spectrometry

Xuefan Gu, Huiwen Zhang, Jun Ye, 2015, Journal of clinical laboratory analysis.

Analysis of genetic mutations in Chinese patients with systemic primary carnitine deficiency.

Xuefan Gu, Huiwen Zhang, Jun Ye, 2014, European journal of medical genetics.

Clinical, biochemical, and molecular analysis of combined methylmalonic acidemia and hyperhomocysteinemia (cblC type) in China

Xuefan Gu, Yanling Yang, Ya-fen Zhang, 2010, Journal of Inherited Metabolic Disease.

[The investigation of differential diagnostic development and incidence of tetrahydrobiopterin deficiency].

X. Gu, Jun Ye, L. Han, 2009, Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine].

Biochemical, molecular and outcome analysis of eight chinese asymptomatic individuals with methyl malonic acidemia detected through newborn screening

Xuefan Gu, Shengnan Wu, Huiwen Zhang, 2015, American journal of medical genetics. Part A.