Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Screening results and genetic features of glucose-6-phosphate dehydrogenase deficiency in 54 025 preterm infants in Chengdu, China].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 1 May 2021

Jiang Zhou, Wang Mei, Tang Li, Li Xiao-Li, Li Chun-Rong, Cheng Xin-Ran

Abstract excerpt

OBJECTIVE: To analyze the screening results of glucose-6-phosphate dehydrogenase (G6PD) deficiency and gene mutation distribution of G6PD deficiency in preterm infants in Chengdu, China, in order to provide a basis for the improvement of G6PD screening process in preterm infants. METHODS: Fluorescent spot test for G6PD deficiency using dried blood spots was used for G6PD screening of 54 025 preterm infants born...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to China
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Infant

Share to Infant, Newborn

Share to Infant, Premature

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 34020738
PMCID: PMC8140343

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Screening results and genetic features of glucose-6-phosphate dehydrogenase deficiency in 54 025 preterm infants in Chengdu, China].PMID 34020738Read ↗

[Correlation analysis of genotypes and the enzymatic activities of glucose-6-phosphate dehydrogenase in neonates in Guangzhou].Semantic proximity Read ↗

Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates.Semantic proximity Read ↗

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017Semantic proximity Read ↗

Incidence and molecular characterization of Glucose-6-Phosphate Dehydrogenase deficiency among neonates for newborn screening in Chaozhou, China.Semantic proximity Read ↗

Molecular epidemiological characteristics, variant spectrum and genotype-phenotype correlation of glucose-6-phosphate dehydrogenase deficiency in China: A population-based multicenter study using newborn screening.Semantic proximity Read ↗

Screening results and mutation frequency analysis of G6PD deficiency in 1,291,274 newborns in Huizhou, China: a twenty-year experience.Semantic proximity Read ↗

[Genetic Mutation Characteristics of Glucose-6-Phosphate Dehydrogenase Deficiency Patients in Wuhan].Semantic proximity Read ↗

Mutation of glucose-6-phosphate dehydrogenase deficiency in Chinese Han children in eastern Fujian.Semantic proximity Read ↗

Molecular genotyping of G6PD mutations for neonates in Ningbo area.Semantic proximity Read ↗

[Phenotypic and genotypic spectra of patients with glucose-6-phosphate dehydrogenase deficiency gene known pathogenic variants: a single-center study].Semantic proximity Read ↗

Mutation spectrum and enzyme profiling of G6PD deficiency in neonates of north India: a prospective study.Semantic proximity Read ↗

[Relationship between glucose-6-phosphate dehydrogenase gene mutations and neonatal jaundice in Naning, Guangxi].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.