Rongyu Chen
Nanning, 530003, China
Last Updated: 09/26/2026
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Found 15 publications
Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 13, 2017
Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: January 08, 2017
A novel compound heterozygous mutation causing 3-methylcrotonyl-CoA carboxylase deficiency
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 01, 2016
Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 13, 2016
Identification of two novel mutations of MUT gene in a Chinese family affected with isolated methylmalonic acidemia
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 10, 2016
Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 25, 2016
A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33.
Journal: Gene
Published: January 25, 2016
Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism.
Journal: Molecular and cellular endocrinology
Published: September 10, 2015
Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism.
Journal: Archives of endocrinology and metabolism
Published: July 13, 2015
PAX8 pathogenic variants in Chinese patients with congenital hypothyroidism.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: July 05, 2015
Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism.
Journal: Journal of endocrinological investigation
Published: July 01, 2015
Last Updated: 09/26/2026