Xiaobao Wei
Liuzhou, China
Last Updated: 09/26/2026
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Found 8 publications
HBA2 Gene Conversion Disrupts Reverse Dot-Blot Hybridization Genotyping: A Prenatal Case of Non-Deletional α-Thalassemia Misdiagnosis.
Journal: Hemoglobin
Published: April 16, 2026
Functional analysis of a novel splice site variant of RAB3GAP2 in a fetus with congenital cataracts.
Functional analysis of a novel splice site variant of RAB3GAP2 in a fetus with congenital cataracts.
Journal: BMC medical genomics
Published: October 04, 2025
Elucidating the pathogenic mechanism of a pedigree with complex rearrangements on chromosome 4 using optical genome mapping technology: a study on the genetics and functional pathways in a child with developmental delay.
Journal: Molecular cytogenetics
Published: July 19, 2025
Novel AK-1 gene variants combined with thalassemia causing rare hereditary non-spherocytic hemolytic anemia in a Chinese family.
Journal: Annals of hematology
Published: December 30, 2024
A Novel Homozygous Synonymous Variant in CCDC134 as a Cause of Osteogenesis Imperfecta Type XXII.
Journal: Clinical genetics
Published: September 12, 2024
Improved Genetic Characterization of Congenital Adrenal Hyperplasia by Long-Read Sequencing Compared with Multiplex Ligation-Dependent Probe Amplification Plus Sanger Sequencing.
Journal: The Journal of molecular diagnostics : JMD
Published: November 16, 2023
Distribution characteristics and clinical phenotype analyses of hemoglobin variants in the Z region of Central Guangxi, Southern China.
Journal: Hematology (Amsterdam, Netherlands)
Published: March 30, 2023
Showing 1-8 of 8
Last Updated: 09/26/2026