Qifei Li
Nanning, China
Last Updated: 09/26/2026
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Found 8 publications
A novel and recurrent KLHL40 pathogenic variants in a Chinese family of multiple affected neonates with nemaline myopathy 8.
Journal: Molecular genetics & genomic medicine
Published: July 01, 2020
Genetic testing and pregnancy outcome of 337 fetuses with urinary system anomalies
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 06, 2019
Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: September 14, 2017
Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound.
Journal: Arquivos brasileiros de cardiologia
Published: July 16, 2017
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
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
Showing 1-8 of 8
Last Updated: 09/26/2026