Fuying Song
Beijing, 100020, China
Last Updated: 09/26/2026
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Found 12 publications
Genetic analysis of a Chinese pedigree affected with Isolated growth hormone deficiency due to variant of CHRHR gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 11, 2026
Clinical and genetic analysis of a child with 46,XX male phenotype due to SOX3 gene duplication
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 01, 2026
Teriparatide for the treatment of primary hypoparathyroidism in children.
Journal: American journal of translational research
Published: January 11, 2026
Growth hormone therapy in children with temple syndrome: the first retrospective study in China.
Journal: BMC pediatrics
Published: December 19, 2025
A Novel Y-Shaped Pegylated Recombinant Human Growth Hormone for Children With Growth Hormone Deficiency.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 11, 2024
Clinical characteristics and genetic analysis of three children with Congenital chlorine diarrhea
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: January 29, 2023
Clinical and genetic analysis of a patient with isolated 17,20 lyase deficiency presenting with pubertal gynecomastia
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 10, 2022
The pharmacokinetic and pharmacodynamic properties and short-term outcome of a novel once-weekly PEGylated recombinant human growth hormone for children with growth hormone deficiency.
Journal: Frontiers in endocrinology
Published: April 17, 2022
Analysis of clinical features and genetic variants among 12 children with Gitelman syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 07, 2021
Clinical and genetic analysis of a child with neonatal severe parathyroidism
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 12, 2020
Next-Generation Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Combined Features of Spherocytosis and Antley-Bixler Syndrome With Genital Anomalies and Disordered Steroidogenesis.
Journal: Frontiers in genetics
Published: November 26, 2019
Allelic variations of glut-1 deficiency syndrome: the chinese experience.
Journal: Pediatric neurology
Published: January 06, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026