Shao-hua Tang

Key Laboratory Of Medical Genetic
Wenzhou, China

Last Updated: 09/26/2026

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Found 11 publications

Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.

Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.

Journal: Molecular genetics & genomic medicine
Published: July 06, 2020

Analysis of MYH3 gene variation and prenatal diagnosis for two pedigrees affected with congenital arthrogryposis

Analysis of MYH3 gene variation and prenatal diagnosis for two pedigrees affected with congenital arthrogryposis

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 29, 2019

Analysis of SACS mutation in a family affected with autosomal recessive spastic ataxia of Charlevoix-Saguenay

Analysis of SACS mutation in a family affected with autosomal recessive spastic ataxia of Charlevoix-Saguenay

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 06, 2019

Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.

Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.

Journal: International journal of pediatric otorhinolaryngology
Published: December 18, 2018

Mutational analysis and prenatal diagnosis in a family affected with hypophosphatemic rickets

Mutational analysis and prenatal diagnosis in a family affected with hypophosphatemic rickets

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 06, 2017

Clearance of free fetal DNA after delivery of fetuses carrying chromosomal aneuploidies

Clearance of free fetal DNA after delivery of fetuses carrying chromosomal aneuploidies

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 12, 2017

Mutation analysis for a Chinese family affected with Escobar syndrome by whole exome sequencing

Mutation analysis for a Chinese family affected with Escobar syndrome by whole exome sequencing

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 12, 2017

Preoperative serum visfatin levels and prognosis of breast cancer among Chinese women.

Preoperative serum visfatin levels and prognosis of breast cancer among Chinese women.

Journal: Peptides
Published: October 27, 2013

Prenatal diagnosis and clinical counseling for fetal chromosomal reciprocal translocations

Prenatal diagnosis and clinical counseling for fetal chromosomal reciprocal translocations

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 01, 2013

SNP-chip technology for identification of origins for prenatally detected marker chromosomes

SNP-chip technology for identification of origins for prenatally detected marker chromosomes

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 09, 2013

First trimester, second trimester, and integrated screening for Down's syndrome in China.

First trimester, second trimester, and integrated screening for Down's syndrome in China.

Journal: Journal of medical screening
Published: June 02, 2012
Showing 1-11 of 11

Last Updated: 09/26/2026