Ruizhu Lin

Phenotype and molecular characteristics in 45 Chinese children with 5α‐reductase type 2 deficiency from South China

Guochang Liu, Li Liu, H. Sheng, 2015, Clinical endocrinology.

Clinical and molecular analysis of 6 Chinese patients with isoleucine metabolism defects: identification of 3 novel mutations in the HSD17B10 and ACAT1 gene

Zhichun Feng, Li Liu, H. Sheng, 2017, Metabolic Brain Disease.

Phenotypic and Molecular Characteristics of Children with Progressive Familial Intrahepatic Cholestasis in South China

Wen Zhang, Li Liu, Yan-na Cai, 2020, Pediatric gastroenterology, hepatology & nutrition.

Separation and identification of underivatized plasma acylcarnitine isomers using liquid chromatography-tandem mass spectrometry for the differential diagnosis of organic acidemias and fatty acid oxidation defects.

X. Fang, Yonglan Huang, Li Liu, 2013, Journal of chromatography. A.

A novel homozygous splice‐site variant of NCAPD2 gene identified in two siblings with primary microcephaly: The second case report

Yunting Lin, C. Zeng, Li Liu, 2019, Clinical genetics.

Clinical, biochemical, neuroimaging and molecular findings of X-linked Adrenoleukodystrophy patients in South China

Yonglan Huang, Li Liu, Li-ping Fan, 2015, Metabolic Brain Disease.