Huamei Hu
Chongqing, China
Last Updated: 09/26/2026
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Found 14 publications
Prenatal diagnosis and genetic analysis: rare familial chromosomal duplications larger than 5 Mb without disease phenotypes.
Journal: Pediatric research
Published: March 26, 2024
Prenatal Diagnosis and Genetic Analysis of 21q21.1-q21.2 Aberrations in Seven Chinese Pedigrees.
Journal: Frontiers in genetics
Published: June 28, 2021
An assessment of the analytical performance of non-invasive prenatal testing (NIPT) in detecting sex chromosome aneuploidies: 34,717-patient sample in a single prenatal diagnosis Centre in China.
Journal: The journal of gene medicine
Published: February 02, 2021
Factors affecting the failure of non-invasive prenatal testing and the feasibility analysis of retesting
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 31, 2020
Positive maternal blood cfDNA test caused by confined placental mosaicism in a case
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 31, 2020
Prenatal diagnosis of familial submicroscopic duplication at 18q22.3 without phenotypic abnormalities.
Journal: Taiwanese journal of obstetrics & gynecology
Published: January 09, 2020
A retrospective analysis the clinic data and follow-up of non-invasive prenatal test in detection of fetal chromosomal aneuploidy in more than 40,000 cases in a single prenatal diagnosis center.
Journal: European journal of medical genetics
Published: December 31, 2019
Detection of fetal trisomy and single gene disease by massively parallel sequencing of extracellular vesicle DNA in maternal plasma: a proof-of-concept validation.
Journal: BMC medical genomics
Published: April 01, 2019
Genome-wide detection of additional fetal chromosomal abnormalities by cell-free DNA testing of 15,626 consecutive pregnant women.
Journal: Science China. Life sciences
Published: May 11, 2018
Prenatal diagnosis of a case with combined Wolf-Hirschhorn syndrome and Jacobsen syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 08, 2015
Targeted next-generation sequencing identification of mutations in patients with disorders of sex development.
Journal: BMC medical genetics
Published: August 01, 2015
Last Updated: 09/26/2026