Yi-feng Yang
Changsha, China
Last Updated: 09/26/2026
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Found 23 publications
The prevalence of laterality defects in patients with congenital heart disease.
Journal: Journal of human genetics
Published: November 23, 2024
Whole exome sequence reveals genetic profiles of primary cardiomyopathy and genotype-phenotype association in Chinese population.
Journal: BMC genomics
Published: February 18, 2024
Identification of a pathogenic SMCHD1 variant in a Chinese patient with bosma arhinia microphthalmia syndrome: a case report.
Journal: BMC medical genomics
Published: October 03, 2023
A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient.
Journal: Journal of human genetics
Published: January 28, 2022
Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome.
Journal: Frontiers in cardiovascular medicine
Published: May 11, 2021
A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient.
Journal: Frontiers in cardiovascular medicine
Published: July 11, 2020
Mutant CARD10 in a family with progressive immunodeficiency and autoimmunity.
Journal: Cellular & molecular immunology
Published: March 15, 2020
19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome.
Journal: Molecular cytogenetics
Published: February 26, 2016
A clinical and molecular analysis of a patient with Emanuel syndrome.
Journal: Molecular medicine reports
Published: November 21, 2015
Novel mutation of EXT2 identified in a large family with multiple osteochondromas.
Journal: Molecular medicine reports
Published: October 17, 2015
Last Updated: 09/26/2026