Xuan G. Shang
Guangzhou, 510515, China
Last Updated: 09/26/2026
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Found 57 publications
Genetic analysis of a fetus with renal dysplasia/hypoplasia due to a variant of GREB1L gene and literature review
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 06, 2026
Genetic dissection of clinical heterogeneity in hemoglobin H patients by targeted long-read sequencing.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: December 11, 2025
Nutritional impacts of dietary selenium and iodine and their interaction on growth performance, antioxidant capacity and bone quality in Longyan ducklings.
Journal: British poultry science
Published: August 11, 2025
Correction: Investigating genotype-phenotype correlation of limb-girdle muscular dystrophy R8: association of clinical severity, protein biological function and protein oligomerization.
Journal: Acta neuropathologica communications
Published: May 06, 2025
Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East Asia.
Journal: Nature communications
Published: February 18, 2025
Application value of long-read sequencing in full characterization of thalassemia-associated structural variations: identifying a novel large segmental duplication and literature review.
Journal: Orphanet journal of rare diseases
Published: January 05, 2025
Investigating genotype-phenotype correlation of limb-girdle muscular dystrophy R8: association of clinical severity, protein biological function and protein oligomerization.
Journal: Acta neuropathologica communications
Published: October 10, 2024
Hb H Disease Caused by Uniparental Disomy: First Report of the αT-Saudiα Mutation in the Chinese Population.
Journal: Mediterranean journal of hematology and infectious diseases
Published: July 28, 2024
Clinical evaluation of target capture sequencing technique for noninvasive prenatal diagnosis of β-thalassemia: A prospective case series.
Journal: Medicine
Published: July 23, 2024
SNPscan Combined With CNVplex as a High-Performance Diagnostic Method for Thalassemia.
Journal: Prenatal diagnosis
Published: March 28, 2024
Precise diagnosis of a hereditary spherocytosis patient with complicated hematological phenotype.
Journal: Molecular genetics and genomics : MGG
Published: November 22, 2023
Last Updated: 09/26/2026