Changshun Yu
Tianjin, China
Last Updated: 09/26/2026
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Found 8 publications
Identification of novel variants in hereditary spherocytosis patients by whole-exome sequencing.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: July 18, 2024
Identification of the synonymous variant c.3141G > A in TNRC6B gene that altered RNA splicing by minigene assay.
Journal: Molecular biology reports
Published: May 13, 2024
Delayed Diagnosis of Spinal Muscular Atrophy in Two Chinese Families due to Novel SMN1 Deletions.
Journal: American journal of medical genetics. Part A
Published: March 23, 2024
Whole exome sequencing approach for identification of the molecular etiology in pediatric patients with hematuria.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: October 05, 2023
Utility of labial salivary gland biopsy in the histological diagnosis of neuronal intranuclear inclusion disease.
Journal: European journal of neurology
Published: August 03, 2023
Identification of two aberrant transcripts by RNA sequencing for a novel variant c.3354 + 5 G > A of MED12 in a Chinese girl with non-syndromic intellectual disability.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: March 18, 2022
Identification of a Novel Deep Intronic Variant by Whole Genome Sequencing Combined With RNA Sequencing in a Chinese Patient With Menkes Disease.
Journal: Frontiers in genetics
Published: January 11, 2022
Hepatitis C virus genotypes and subtypes circulating in Mainland China.
Journal: Emerging microbes & infections
Published: February 20, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026