Cuize Yao
Guangzhou, China
Last Updated: 09/26/2026
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Found 18 publications
High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases.
Journal: Journal of translational medicine
Published: April 07, 2024
Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families.
Journal: Human genomics
Published: September 11, 2023
Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia.
Journal: Scientific reports
Published: May 10, 2023
Hb Chapel Hill or Alpha2 74(EF3) Asp>Gly, a mildly unstable variant found in a Chinese family.
Journal: Hematology (Amsterdam, Netherlands)
Published: March 20, 2023
Hb Q-Thailand heterozygosity unlinked with the (-α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses.
Journal: Hematology (Amsterdam, Netherlands)
Published: March 03, 2023
First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families.
Journal: Hematology (Amsterdam, Netherlands)
Published: August 08, 2022
The -α3.7III subtype of α+-thalassemia was identified in China.
Journal: Hematology (Amsterdam, Netherlands)
Published: August 02, 2022
The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review.
Journal: Hematology (Amsterdam, Netherlands)
Published: February 22, 2022
Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR.
Journal: Hematology (Amsterdam, Netherlands)
Published: January 31, 2022
Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C).
Journal: The Journal of international medical research
Published: August 02, 2021
Last Updated: 09/26/2026