Nana Song
Shenzhen, China
Last Updated: 09/26/2026
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Found 8 publications
Genome Sequencing Unveils the Role of Copy Number Variants in Hearing Loss and Identifies Novel Deletions With Founder Effect in the DFNB1 Locus.
Journal: Human mutation
Published: May 18, 2024
Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomy.
Journal: American journal of obstetrics & gynecology MFM
Published: October 20, 2022
Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss.
Journal: Human genetics
Published: March 16, 2022
Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss.
Journal: BMC medical genomics
Published: February 28, 2022
VIP-HL: Semi-automated ACMG/AMP variant interpretation platform for genetic hearing loss.
Journal: Human mutation
Published: November 30, 2020
Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach.
Journal: Scientific reports
Published: October 12, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026