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

α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases.

Hemoglobin - 1 May 2017

Zhang Qiang, Xu Mingli, Zhou Wanjun, Fan Xin

Abstract excerpt

A novel 811 bp deletion was first identified in two families of Nanning City, Guangxi Zhuang Autonomous Region, People's Republic of China (PRC). The molecular basis of this anomaly is a deletion from NG_000006.1: g.32945_33755, and is 20 bp upstream of the translation initiation codon of HBA2. From analyses of the blood indices of the two probands, the 811 bp deletion is an α+-thalassemia (α+-thal). This is the...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to alpha-Globins
Share to alpha-Thalassemia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Multigene Family

Share to Sequence Analysis, DNA

Share to Sequence Deletion

Source

Identifiers

PMID: 28840763
DOI: 10.1080/03630269.2017.1371035

Genes

HBA2

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

α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases.PMID 28840763Read ↗

Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family.Semantic proximity Read ↗

Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis.Semantic proximity Read ↗

A Novel Mutation at HBA1: c.349G>T Causing α-Thalassemia in a Chinese Family.Semantic proximity Read ↗

The diagnosis and molecular analysis of a novel 21.9kb deletion (Qinzhou type deletion) causing α+ thalassemia.Semantic proximity Read ↗

Identification of a novel 10.3 kb deletion causing α0-thalassemia by third-generation sequencing: Pedigree analysis and genetic diagnosis.Semantic proximity Read ↗

A novel 6.3 kb deletion and the Rare 27.6 kb Deletion Causing α+-Thalassemia in two Chinese Patients.Semantic proximity Read ↗

Case report: Long-read sequencing identified a novel 14.9-kb deletion of the α-globin gene locus in a family with α-thalassemia in ChinaSemantic proximity Read ↗

A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.Semantic proximity Read ↗

Analysis of genotype-phenotype correlation in patients with α-thalassemia from Fujian province, Southeastern China.Semantic proximity Read ↗

The diagnosis and molecular analysis of a novel 27.2 kb deletion causing α0-thalassemia.Semantic proximity Read ↗

Identification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family.Semantic proximity Read ↗

Genotypic and phenotypic characterization of rare globin variants in Northern Guangxi, China.Semantic proximity Read ↗

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