Lanping Hu

Hunan Provincial Key Laboratory Of Regional Hereditary Birth Defects Prevention And Control
Changsha, 410007, China

Last Updated: 09/26/2026

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Found 11 publications

Genetic rare disease prevention and control: Family-based screening and reproductive interventions in Changsha.

Genetic rare disease prevention and control: Family-based screening and reproductive interventions in Changsha.

Journal: HGG advances

Published: February 06, 2025

Cost-effectiveness of different screening strategies for Down syndrome: a real-world analysis in 140,472 women.

Cost-effectiveness of different screening strategies for Down syndrome: a real-world analysis in 140,472 women.

Journal: Frontiers in public health

Published: November 27, 2024

Determining the origin of genome aberrations improves the positive predictive value of NIPT for 22q11.2 deletion syndrome.

Determining the origin of genome aberrations improves the positive predictive value of NIPT for 22q11.2 deletion syndrome.

Journal: Scientific reports

Published: November 22, 2024

The genetics and clinical outcomes in 151 cases of fetal growth restriction: A Chinese single-center study.

The genetics and clinical outcomes in 151 cases of fetal growth restriction: A Chinese single-center study.

Journal: European journal of obstetrics, gynecology, and reproductive biology

Published: November 28, 2023

Comparison of Third-Generation Sequencing and Routine Polymerase Chain Reaction in Genetic Analysis of Thalassemia.

Comparison of Third-Generation Sequencing and Routine Polymerase Chain Reaction in Genetic Analysis of Thalassemia.

Journal: Archives of pathology & laboratory medicine

Published: February 21, 2023

Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomy.

Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomy.

Journal: American journal of obstetrics & gynecology MFM

Published: October 20, 2022

Prenatal genetic diagnosis of tetrasomy 18p from maternal trisomy 18p: a case report.

Prenatal genetic diagnosis of tetrasomy 18p from maternal trisomy 18p: a case report.

Journal: Molecular cytogenetics

Published: October 16, 2021

Value of chromosomal microarray analysis for the prenatal diagnosis of pregnancy with high risk signaled by non-invasive prenatal testing

Value of chromosomal microarray analysis for the prenatal diagnosis of pregnancy with high risk signaled by non-invasive prenatal testing

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: June 07, 2021

A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA).

A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA).

Journal: The Journal of molecular diagnostics : JMD

Published: January 18, 2021

Diagnosis of a fetus with a de novo 16q partial trisomy syndrome

Diagnosis of a fetus with a de novo 16q partial trisomy syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 14, 2020

Prevalence and spectrum of thalassaemia in Changsha, Hunan province, China: discussion of an innovative screening strategy.

Prevalence and spectrum of thalassaemia in Changsha, Hunan province, China: discussion of an innovative screening strategy.

Journal: Journal of genetics

Published: July 05, 2017

Showing 1-11 of 11

Last Updated: 09/26/2026