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

[Gene Sequencing Analysis of 5 Patients with D Variant in Guangxi -Attached 1 Case of D Variant with New Allele].

Zhongguo shi yan xue ye xue za zhi - 1 Apr 2026

Xie Hui-Qiong, Huang Hui-Ni, Huang Hua-Li, Wei Yue-Rong, Li Si-Na, Wu Chun-Le, Li Hao, Mo Zhu-Ning, Li Hai-Lan

Abstract excerpt

OBJECTIVE: To assist the identification of clinical D variants using genetic testing technology. METHODS: Five blood samples of patients with Rh D blood group with weakly positive/negative serological manifestations received by the Blood Transfusion Department of the Guangxi Zhuang Autonomous Region People's Hospital from January 2022 to December 2023 were randomly collected, and all of them were subjected to...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to RHD gene

Share to Genotype

Share to Mutation

Share to Rh-Hr Blood-Group System

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 42227439
DOI: 10.19746/j.cnki.issn1009-2137.2026.02.020

Genes

RHD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Gene Sequencing Analysis of 5 Patients with D Variant in Guangxi -Attached 1 Case of D Variant with New Allele].PMID 42227439Read ↗

[RHD Genotyping Characteristics of RhD-Negative Blood Donors in Wuhu Area].Semantic proximity Read ↗

An RHD gene variant, common in southern Chinese Han, involves a short 688 bp deletion and a long 21.8 kb insertion in the RHD exon 10 non-coding region, affecting the accuracy of red cell genotyping.Semantic proximity Read ↗

Identification and pedigree analysis of a hidden partial D antigen with rare RHD*DV.1 allele.Semantic proximity Read ↗

[Gene Mutation Analysis of an Individual with a RHD Variant RHD*DV.5 and RHD Negative Gene Heterozygote].Semantic proximity Read ↗

Molecular and computational analysis of 45 samples with a serologic weak D phenotype detected among 132,479 blood donors in northeast China.Semantic proximity Read ↗

A Review of the Literature Organized Into a New Database: RHeference.Semantic proximity Read ↗

Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population.Semantic proximity Read ↗

Frequency of RHD variants among blood donors in the central region of Iran, Yazd province.Semantic proximity Read ↗

Five-Years Review of RHCE Alleles Detected after Weak and/or Discrepant C Results in Southern France.Semantic proximity Read ↗

Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare alleles.Semantic proximity Read ↗

Clinical and laboratory update on the DEL variant.Semantic proximity Read ↗

Overview of the serologic and molecular basis of D variants with a focus on D variants in the Indian population.Semantic proximity Read ↗

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