Yao Chen

发表

Mutation of glucose-6-phosphate dehydrogenase deficiency in Chinese Han children in eastern Fujian

Jing Wang, Hua Li, Wenbin Zhu, 2018, Medicine.

[Risk factors of 125 cases of neonatal congenital hypothyroidism during perinatal period].

Jing Wang, Wenbin Zhu, Jinying Luo, 2015, Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi.

A novel dual oxidase maturation factor 2 gene mutation for congenital hypothyroidism.

L. Lan, Jing Wang, Liyong Yang, 2013, International journal of molecular medicine.

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017

Hua Tang, Zhidai Liu, Peng-hui Zhang, 2020, Human mutation.

Peripheral blood level of 17-hydroxyprogesterone in neonates and influencing factors

Jing Wang, Wenbin Zhu, Yueqing Su, 2015 .

A verification of the application of the non-derivatized mass spectrometry method in newborns screening of metabolic disorders

Wenbin Zhu, Yao Chen, Hong Zhao, 2019, Medicine.

Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian

Wenbin Zhu, Guanghua Liu, Yao Chen, 2021, Medicine.

Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study

Jing Wang, Wenbin Zhu, Changyi Yang, 2018, BioMed research international.

Gene spectrum and clinical traits of 10 patients with primary carnitine deficiency

Wenbin Zhu, Guanghua Liu, Yao Chen, 2021, Molecular genetics & genomic medicine.

Newborn Screening of 6 Lysosomal Storage Disorders by Tandem Mass Spectrometry.

Wenbin Zhu, Peiran Zhao, Yao Chen, 2023, Clinical pediatrics.