Xinhua H. Tang

NHC Key Laboratory Of Health Birth And Birth Defect Prevention In Western China, Yunnan Provincial Key Laboratory For Birth Defects And Genetic Diseases
Kunming, 650032, China

Last Updated: 09/26/2026

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Found 14 publications

Efficiency of CNV-seq in detecting fetal DMD gene deletion or duplication in prenatal diagnosis

Efficiency of CNV-seq in detecting fetal DMD gene deletion or duplication in prenatal diagnosis

Journal: Zhonghua fu chan ke za zhi

Published: April 21, 2024

Molecular Mechanisms of Medicinal Plant Securinega suffruticosa-derived Compound Securinine against Spinal Muscular Atrophy based on Network Pharmacology and Experimental Verification.

Molecular Mechanisms of Medicinal Plant Securinega suffruticosa-derived Compound Securinine against Spinal Muscular Atrophy based on Network Pharmacology and Experimental Verification.

Journal: Current pharmaceutical design

Published: November 24, 2023

The relationship of maternal polymorphisms of genes related to meiosis and DNA damage repair with fetal chromosomal stability.

The relationship of maternal polymorphisms of genes related to meiosis and DNA damage repair with fetal chromosomal stability.

Journal: Journal of perinatal medicine

Published: December 22, 2022

Maternal genetic polymorphisms in the major mitotic checkpoint genes MAD1L1 and MAD2L1 associated with the risk of survival in abnormal chromosomal fetuses.

Maternal genetic polymorphisms in the major mitotic checkpoint genes MAD1L1 and MAD2L1 associated with the risk of survival in abnormal chromosomal fetuses.

Journal: Frontiers in genetics

Published: November 22, 2022

Ultrasonographic classification of 26 cases of fetal umbilical-portal-systemic venous shunts and the correlations with fetal chromosomal abnormalities.

Ultrasonographic classification of 26 cases of fetal umbilical-portal-systemic venous shunts and the correlations with fetal chromosomal abnormalities.

Journal: BMC pregnancy and childbirth

Published: October 03, 2022

Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.

Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.

Journal: BMC pregnancy and childbirth

Published: November 19, 2020

Result of carrier screening for spinal muscular atrophy among 3049 reproductive-age individuals from Yunnan region

Result of carrier screening for spinal muscular atrophy among 3049 reproductive-age individuals from Yunnan region

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

Published: March 29, 2020

The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study.

The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study.

Journal: Medicine

Published: February 04, 2020

First-trimester maternal serum alpha-fetoprotein is not a good predictor for adverse pregnancy outcomes: a retrospective study of 3325 cases.

First-trimester maternal serum alpha-fetoprotein is not a good predictor for adverse pregnancy outcomes: a retrospective study of 3325 cases.

Journal: BMC pregnancy and childbirth

Published: September 10, 2019

Genetic analysis and prenatal diagnosis for a pregnant woman with an unbalanced t(1;2), t(6;7) translocation and intellectual disability

Genetic analysis and prenatal diagnosis for a pregnant woman with an unbalanced t(1;2), t(6;7) translocation and intellectual disability

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

Published: August 05, 2017

Application of BoBs technique for detecting common chromosome microdeletion and microduplication syndromes

Application of BoBs technique for detecting common chromosome microdeletion and microduplication syndromes

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

Published: July 26, 2016

Prenatal diagnosis of chromosome abnormalities and nine microdeletion syndromes using both traditional karyotyping and BoBs

Prenatal diagnosis of chromosome abnormalities and nine microdeletion syndromes using both traditional karyotyping and BoBs

Journal: Zhonghua fu chan ke za zhi

Published: June 04, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026