Chuanxin Feng
Nanchang, China
Last Updated: 09/26/2026
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Found 8 publications
Chromosomal structural abnormalities and tissue-specific mosaicism: insights into false-negative noninvasive prenatal testing.
Journal: Frontiers in genetics
Published: April 02, 2026
A novel splicing variant in TECTA associated with prelingual autosomal dominant nonsyndromic hearing loss via dominant-negative effect.
Journal: Human molecular genetics
Published: April 02, 2025
Exploring the correlation between homocysteine, red blood cell folate and MTHFRC677T genotypes with female infertility.
Journal: Biomarkers in medicine
Published: September 10, 2024
Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA.
Journal: Human molecular genetics
Published: January 09, 2024
Identification of two novel and one rare mutation in DYRK1A and prenatal diagnoses in three Chinese families with intellectual Disability-7.
Journal: Frontiers in genetics
Published: September 08, 2023
Identification of five novel SCN1A variants.
Journal: Frontiers in behavioral neuroscience
Published: August 04, 2023
Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center study.
Journal: Orphanet journal of rare diseases
Published: June 23, 2023
Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, China.
Journal: Frontiers in genetics
Published: October 19, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026