Wenjuan Qiu
9PUBLICATIONS
16CO-AUTHORS
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Publications (9)
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|Jul 25, 2024
Long-Read Sequencing Solves Complex Structure of CYP21A2 in a Large 21-Hydroxylase Deficiency Cohort.Ruifang Wang, Xiaomei Luo, Yu Sun
|Feb 16, 2024
Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome.Taozi Du, Yu Xia, Chengkai Sun
|Aug 16, 2023
Genetic and phenotypic spectrum of non-21-hydroxylase-deficiency primary adrenal insufficiency in childhood: data from 111 Chinese patients.Ying Duan, Wanqi Zheng, Yu Xia
|Jun 14, 2023
Evaluation of the clinical, biochemical, genotype and prognosis of mut-type methylmalonic acidemia in 365 Chinese cases.Lili Liang, Shiying Ling, Yue Yu
|May 26, 2023
Clinical and genetic characteristics of 42 Chinese paediatric patients with X-linked adrenal hypoplasia congenita.Wanqi Zheng, Ying Duan, Yu Xia
|Feb 10, 2022
Diagnosis and follow-up of glycogen storage disease (GSD) type VI from the largest GSD center in China.Xiaomei Luo, Ying Duan, Di Fang
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