Xi Wang
NHC Key Laboratory Of Endocrinology, Peking Union Medical College Hospital, Peking Union Medical College
Beijing, 100730, China
Beijing, 100730, China
Last Updated: 09/26/2026
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Found 9 publications
Novel CYP17A1 variants and functional validation in a large Chinese cohort of complete 17α-hydroxylase deficiency.
Journal: The Journal of clinical endocrinology and metabolism
Published: November 20, 2025
Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency Detected by Long-Read Sequencing and Phenotypes Correlation.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 04, 2024
CYP17A1 Pathogenic Variants in 26 Chinese Patients With 17α-Hydroxylase Deficiency by Targeted Long-Read Sequencing.
Journal: The Journal of clinical endocrinology and metabolism
Published: December 08, 2023
The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant.
Journal: Frontiers in endocrinology
Published: August 10, 2022
High prevalence of hypertension and target organ damage in patients with 11β-hydroxylase deficiency.
High prevalence of hypertension and target organ damage in patients with 11β-hydroxylase deficiency.
Journal: Clinical endocrinology
Published: August 08, 2021
Bone mineral density and trabecular bone score in patients with 21-hydroxylase deficiency after glucocorticoid treatment.
Journal: Clinical endocrinology
Published: September 12, 2020
The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency.
Journal: The Journal of clinical endocrinology and metabolism
Published: October 31, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026