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 and prenatal diagnosis of the haemoglobinopathies.

Bailliere's clinical haematology - 1 Mar 1993

Cao A, Rosatelli M C

Abstract excerpt

In this paper we have reviewed the social and technical aspects of carrier screening and prenatal diagnosis of the inherited haemoglobinopathies. The characteristics of programmes based on carrier screening and prenatal diagnosis ongoing in a number of at-risk Mediterranean populations have been described. The most relevant and common aspects of these programmes are the continuous educational campaign directed to...

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 DNA Restriction Enzymes
Share to Globins

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mass Screening

Share to Mutation

Share to Phenotype

Share to Pregnancy

Share to Prenatal Diagnosis

Source

Identifiers

PMID: 8394756
DOI: 10.1016/s0950-3536(05)80072-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening and prenatal diagnosis of the haemoglobinopathies.PMID 8394756Read ↗

Prenatal diagnosis of hemoglobin disorders: present and future strategies.Semantic proximity Read ↗

Prenatal diagnosis of beta-thalassaemia and sickle cell anaemia in Turkey.Semantic proximity Read ↗

Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methods.Semantic proximity Read ↗

Prenatal molecular diagnosis of beta-thalassemia: report on the first two cases in Romania.Semantic proximity Read ↗

8 Prenatal diagnosis and screening of the haemoglobinopathiesSemantic proximity Read ↗

Rapid detection of fetal Mendelian disorders: thalassemia and sickle cell syndromes.Semantic proximity Read ↗

Control of beta-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experience.Semantic proximity Read ↗

Thalassaemia screening in pregnancySemantic proximity Read ↗

Antenatal diagnosis of beta-thalassemia in Sardinia.Semantic proximity Read ↗

Carrier screening and prenatal diagnosis of beta-thalassemia.Semantic proximity Read ↗

Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis).Semantic proximity Read ↗

Prenatal diagnosis of ?-thalassaemia and other haemoglobinopathies in IndiaSemantic proximity Read ↗

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