Associated Papers
Association between G6PD gene variants and adverse pregnancy outcomes.
Guo D et al.
Bmc Pregnancy and Childbirth, 2026
Screening, genetic analysis, and clinical transfusion implications of thalassaemia and glucose-6-phosphate dehydrogenase deficiency in blood donors.
Chen ZX et al.
Transfusion Medicine (oxford, England), 2025
A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country.
Aly NH et al.
Blood Cells, Molecules & Diseases, 2023
Etiology analysis for term newborns with severe hyperbilirubinemia in eastern Guangdong of China.
Xu JX et al.
World Journal of Clinical Cases, 2023
Etiology analysis and G6PD deficiency for term infants with jaundice in Yangjiang of western Guangdong.
Yang YK et al.
Frontiers in Pediatrics, 2023
Molecular epidemiological investigation of G6PD deficiency in Yangjiang region, western Guangdong province.
Liang HF et al.
Frontiers in Genetics, 2023
Glucose-6-phosphate dehydrogenase deficiency screening and gene analysis in blood donors of Guangdong province.
Liang HF et al.
Hematology (amsterdam, Netherlands), 2022
Identification of a Novel Hb H Disease with Glucose-6-Phosphate Dehydrogenase Deficiency Using Whole Genome Sequencing.
Ren ZM et al.
Hemoglobin, 2022
UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice.
Yang Z et al.
Frontiers in Pediatrics, 2022
Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong.
Xu JX et al.
Bmc Pediatrics, 2021
Epidemiology, evolutionary origin, and malaria-induced positive selection effects of G6PD-deficient alleles in Chinese populations.
Zheng Y et al.
Molecular Genetics & Genomic Medicine, 2020
Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency in the Shenzhen Population.
Gao J et al.
Human Heredity, 2020
High resolution melting curve analysis enables rapid and reliable detection of G6PD variants in heterozygous females.
Islam MT et al.
Bmc Genetics, 2018
STARD-rapid screening for the 6 most common G6PD gene mutations in the Chinese population using the amplification refractory mutation system combined with melting curve analysis.
Fan Z et al.
Medicine, 2018
Large cohort screening of G6PD deficiency and the mutational spectrum in the Dongguan District in Southern China.
Peng Q et al.
Plos One, 2015
Gold nanostructures for the multiplex detection of glucose-6-phosphate dehydrogenase gene mutations.
Seow N et al.
Analytical Biochemistry, 2014
A reverse dot blot assay for the expanded screening of eleven Chinese G6PD mutations.
Lu X et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2013
Rapid and reliable detection of glucose-6-phosphate dehydrogenase (G6PD) gene mutations in Han Chinese using high-resolution melting analysis.
Yan JB et al.
The Journal of Molecular Diagnostics : Jmd, 2010
Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations.
Yan T et al.
Haematologica, 2006
[Identification of G6PD gene variants from Hakka population in Guangdong province].
Yu GL et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2004
[The preliminary study on the gene mutations of sixty patients with G6PD deficiency in Yunnan province].
Yang Z et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2000
Development and evaluation of a reverse dot blot assay for the simultaneous detection of six common Chinese G6PD mutations and one polymorphism.
Li L et al.
Blood Cells, Molecules & Diseases, 0
Association of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients.
El Sissy MH et al.
Hemoglobin, 0