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

Hydrops fetalis associated with homozygosity for Hb Adana [alpha59(E8)Gly-->Asp (alpha2)].

Hemoglobin - 1 Jan 2010

Nainggolan Ita M, Harahap Alida, Setianingsih Iswari

Abstract excerpt

We describe cases of hydrops fetalis associated with nondeletional alpha-thalassemia (alpha-thal), in three unrelated Indonesian families. The genotypes of the fetuses and their parents were generated by DNA sequencing and by a polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP)-based method to rapidly identify mutations detected by sequencing. Two of the fetuses had hydrops fetalis and...

Read the complete abstract on PubMed

Topics

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

Share to Codon
Share to DNA
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Hemoglobins, Abnormal

Share to Homozygote

Share to Hydrops Fetalis

Share to Polymorphism, Restriction Fragment Length

Source

Open in PubMed Open full text

Identifiers

PMID: 20642338
DOI: 10.3109/03630269.2010.493405
PMCID: PMC2942774

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hydrops fetalis associated with homozygosity for Hb Adana [alpha59(E8)Gly-->Asp (alpha2)].PMID 20642338Read ↗

Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional α(+)-thalassemia mutations: diverse hematological and clinical features.Semantic proximity Read ↗

Molecular analysis of abnormal hemoglobins in beta chain in Aegean region of Turkey and first reports of hemoglobin Andrew-Minneapolis and Hb Hinsdale from Turkey.Semantic proximity Read ↗

Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care ProblemSemantic proximity Read ↗

The First Compound Heterozygosity for Two Different α-Thalassemia Determinants Causes Hb Bart's Hydrops Fetalis in a Chinese Family.Semantic proximity Read ↗

A rare thalassemic syndrome caused by interaction of Hb Adana [alpha59(E8)Gly-->Asp] with an alpha+-thalassemia deletion: clinical aspects in two cases.Semantic proximity Read ↗

Molecular defects in Hb H hydrops fetalis.Semantic proximity Read ↗

Microsatellite markers within --SEA breakpoints for prenatal diagnosis of HbBarts hydrops fetalis.Semantic proximity Read ↗

Haemoglobin H hydrops fetalis syndrome associated with homozygosity for the alpha2-globin gene polyadenylation signal mutation AATAAA-->AATA- -.Semantic proximity Read ↗

Molecular prenatal diagnosis of alpha-thalassemia using real-time and multiplex polymerase chain reaction methods.Semantic proximity Read ↗

Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis.Semantic proximity Read ↗

A Rare Hemoglobinopathy Duo: Hb ADANA x Hb SEA in a One-Year-Old PatientSemantic proximity Read ↗

Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.Semantic proximity Read ↗

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