Bo Gao

28 Fuxing Road
Beijing, 100853, China

Last Updated: 09/26/2026

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Found 14 publications

Clinical validation of 4K three-dimensional exoscope system in stapedotomy: a retrospective cohort study.

Clinical validation of 4K three-dimensional exoscope system in stapedotomy: a retrospective cohort study.

Journal: Frontiers in surgery

Published: April 15, 2026

An in situ non-contact 3D microscopic measurement system for temporal bone anatomy based on stereo imaging.

An in situ non-contact 3D microscopic measurement system for temporal bone anatomy based on stereo imaging.

Journal: Scientific reports

Published: September 23, 2025

Novel autosomal dominant syndromic hearing loss caused by COL4A2 -related basement membrane dysfunction of cochlear capillaries and microcirculation disturbance.

Novel autosomal dominant syndromic hearing loss caused by COL4A2 -related basement membrane dysfunction of cochlear capillaries and microcirculation disturbance.

Journal: Chinese medical journal

Published: November 09, 2024

Single-Molecule Counting for Noninvasive Prenatal Diagnosis of Autosomal Recessive Hearing Loss in at-Risk Families: A Proof-of-Concept Study.

Single-Molecule Counting for Noninvasive Prenatal Diagnosis of Autosomal Recessive Hearing Loss in at-Risk Families: A Proof-of-Concept Study.

Journal: The Journal of molecular diagnostics : JMD

Published: October 31, 2024

Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles: A Universal and Dependable Noninvasive Prenatal Diagnosis Method Applied to Autosomal Recessive Nonsyndromic Hearing Loss in At-Risk Families.

Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles: A Universal and Dependable Noninvasive Prenatal Diagnosis Method Applied to Autosomal Recessive Nonsyndromic Hearing Loss in At-Risk Families.

Journal: The Journal of molecular diagnostics : JMD

Published: November 07, 2023

A capture-based method of prenatal cell-free DNA screening for autosomal recessive non-syndromic hearing loss.

A capture-based method of prenatal cell-free DNA screening for autosomal recessive non-syndromic hearing loss.

Journal: Prenatal diagnosis

Published: October 23, 2023

Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.

Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.

Journal: Journal of human genetics

Published: February 22, 2022

Comparison of endoscopic and microscopic management of attic cholesteatoma: A randomized controlled trial.

Comparison of endoscopic and microscopic management of attic cholesteatoma: A randomized controlled trial.

Journal: American journal of otolaryngology

Published: June 28, 2021

Analysis of genotype-phenotype relationships in 90 Chinese probands with Waardenburg syndrome.

Analysis of genotype-phenotype relationships in 90 Chinese probands with Waardenburg syndrome.

Journal: Human genetics

Published: April 08, 2021

Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing.

Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing.

Journal: Bioscience reports

Published: October 28, 2020

Application of multiplanar reconstruction of spiral CT in the diagnosis and treatment of enlarged vestibular aqueducts.

Application of multiplanar reconstruction of spiral CT in the diagnosis and treatment of enlarged vestibular aqueducts.

Journal: Acta oto-laryngologica

Published: May 25, 2019

Genotype-phenotype variability in Chinese cases of Treacher Collins syndrome.

Genotype-phenotype variability in Chinese cases of Treacher Collins syndrome.

Journal: Acta oto-laryngologica

Published: May 21, 2019

Showing 1-12 of 14

Last Updated: 09/26/2026