Yuying Jiang
Quanzhou, China
Last Updated: 09/26/2026
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Found 45 publications
Molecular Epidemiology of δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin (HPFH) in the Quanzhou Childbearing-Age Population, China.
Journal: Hemoglobin
Published: July 13, 2026
Identification of a Rare β-Globin Chain Hemoglobin Variant: HBB: C.24G > C (Glu7Asp).
Journal: Hemoglobin
Published: December 16, 2025
Optical genome mapping of a complex structural rearrangement family line on chromosome 18.
Journal: Hereditas
Published: August 04, 2025
Prenatal Diagnosis and Functional Analysis of Two Compound Heterozygous Variants in the KLHL40 Gene Causing Nemaline Myopathy 8.
Journal: Molecular genetics & genomic medicine
Published: June 20, 2025
Whole Exome Sequencing Revealing a Novel PBX1 Gene Variant in a Chinese Family Causing Recurrent Neonatal Death.
Journal: Birth defects research
Published: March 21, 2024
Molecular cytogenetic characterization of isolated recurrent 4q35.2 microduplication in Chinese population: a seven-year single-center retrospective study.
Journal: BMC pregnancy and childbirth
Published: February 09, 2024
Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study.
Journal: Molecular cytogenetics
Published: December 29, 2023
Prenatal diagnosis of fetuses with absent/hypoplastic nasal bone in second-trimester using chromosomal microarray analysis.
Journal: Birth defects research
Published: December 06, 2023
Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing.
Journal: Scientific reports
Published: October 05, 2023
Initial clinical and molecular investigation of 20q13.33 microdeletion with 17q25.3/14q32.31q32.33 microduplication in Chinese pediatric patients.
Journal: Molecular genetics & genomic medicine
Published: September 30, 2023
Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study.
Journal: Scientific reports
Published: September 30, 2023
Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese population.
Journal: Molecular genetics & genomic medicine
Published: September 23, 2023
Last Updated: 09/26/2026