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

A case of beta thalassemia major detected using HPLC in a child of Chinese ancestry.

Clinical biochemistry - 1 Jun 2000

Berendt H L, Blakney G B, Clarke G M, Higgins T N

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to beta-Thalassemia
Share to Blood Cell Count
Share to China
Share to Chromatography, High Pressure Liquid

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fetal Hemoglobin

Share to Hemoglobin A2

Share to Homozygote

Share to Infant

Source

Identifiers

PMID: 10936591
DOI: 10.1016/s0009-9120(00)00066-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of beta thalassemia major detected using HPLC in a child of Chinese ancestry.PMID 10936591Read ↗

Diagnostic Dilemma of Hemoglobinopathies Using High Performance Liquid Chromatography Alone: A Case Report from a Resource-Constrained Setting.Semantic proximity Read ↗

HPLC in Characterization of Hemoglobin Profile in Thalassemia Syndromes and Hemoglobinopathies: A Clinicohematological CorrelationSemantic proximity Read ↗

Two cases of homozygous alpha0-thalassemia diagnosed prenatally in pregnancies at risk for beta-thalassemia in China.Semantic proximity Read ↗

Heterozygous β-thalassemia with complete absence of hemoglobin A2 in a Chinese adult.Semantic proximity Read ↗

β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population.Semantic proximity Read ↗

Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLCSemantic proximity Read ↗

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

Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLC.Semantic proximity Read ↗

The Unexpected Detection of a Novel Mutation in a Patient with Hb G-Taipei During Glycated Hemoglobin Test.Semantic proximity Read ↗

Rapid, simultaneous genotyping of five common Southeast Asian beta-thalassemia mutations by multiplex minisequencing and denaturing HPLC.Semantic proximity Read ↗

Case series of HbQ-India, a rare alpha globin variant in a referral laboratory setting in South India.Semantic proximity Read ↗

Rapid detection of an a thalassemia variant (Hb Quong Sze).Semantic proximity Read ↗

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