Hongfei Kang

Zhengzhou, China

Last Updated: 09/26/2026

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Found 9 publications

Clinical application of whole exome sequencing (WES) in the genetic diagnosis of 768 Chinese patients with bilateral hearing loss.

Clinical application of whole exome sequencing (WES) in the genetic diagnosis of 768 Chinese patients with bilateral hearing loss.

Journal: European journal of human genetics : EJHG
Published: February 06, 2025

Genetic testing and prenatal diagnosis for a Chinese pedigree affected with Waardenburg syndrome type 4C due to heterozygous deletion of SOX10 gene

Genetic testing and prenatal diagnosis for a Chinese pedigree affected with Waardenburg syndrome type 4C due to heterozygous deletion of SOX10 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 31, 2023

Genetic diagnosis of Branchio-Oto syndrome pedigree due to a de novo heterozygous deletion of EYA1 gene

Genetic diagnosis of Branchio-Oto syndrome pedigree due to a de novo heterozygous deletion of EYA1 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 29, 2023

Diagnosis of a Chinese pedigree affected with autosomal recessive deafness 4 with enlarged vestibular aqueduct due to compound heterozygous variants of FOXI1 gene

Diagnosis of a Chinese pedigree affected with autosomal recessive deafness 4 with enlarged vestibular aqueduct due to compound heterozygous variants of FOXI1 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 02, 2022

Genetic and prenatal diagnosis of a Chinese pedigree with autosomal recessive Wolfram syndrome 1 due to compound heterozygous variants of WFS1 gene

Genetic and prenatal diagnosis of a Chinese pedigree with autosomal recessive Wolfram syndrome 1 due to compound heterozygous variants of WFS1 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 10, 2022

Genetic diagnosis of a pedigree affected with Usher syndrome type 1D/F

Genetic diagnosis of a pedigree affected with Usher syndrome type 1D/F

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 09, 2021

Genetic testing of a Chinese pedigree affected with non-syndromic autosomal dominant deafness 15

Genetic testing of a Chinese pedigree affected with non-syndromic autosomal dominant deafness 15

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 11, 2021

FVIII inhibitor risk correlated with F8 gene variants in 296 unrelated male Chinese patients with haemophilia A.

FVIII inhibitor risk correlated with F8 gene variants in 296 unrelated male Chinese patients with haemophilia A.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: March 16, 2020

Genetic and prenatal diagnosis of a retinitis pigmentosa pedigree

Genetic and prenatal diagnosis of a retinitis pigmentosa pedigree

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 14, 2018
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Last Updated: 09/26/2026