Shiying Ling
1665 KongJiang Road
Shanghai, 200092, China
Shanghai, 200092, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Clinical spectrum and molecular basis in 19 Chinese patients with 46, XY disorder of sexual development caused by NR5A1 mutations.
Journal: Orphanet journal of rare diseases
Published: August 04, 2024
Long-term follow-up of Chinese patients with methylmalonic acidemia of the cblC and mut subtypes.
Journal: Pediatric research
Published: January 31, 2024
Research progress on the prognosis of patients with various types of Methylmalonic acidemia
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 27, 2023
Late-onset cblC defect: clinical, biochemical and molecular analysis.
Journal: Orphanet journal of rare diseases
Published: April 19, 2023
Clinical characteristics and genotype analysis of five infants with cblX type of methylmalonic acidemia.
Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences
Published: October 08, 2022
Clinical, biochemical, and genetic analysis of 28 Chinese patients with holocarboxylase synthetase deficiency.
Journal: Orphanet journal of rare diseases
Published: September 27, 2022
Clinical features and outcomes of patients with cblC type methylmalonic acidemia carrying gene c.609G>A mutation.
Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences
Published: October 27, 2021
Showing 1-10 of 10
Last Updated: 09/26/2026