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

[Abnormal haemoglobins in the newborn human population of Costa Rica].

Revista de biologia tropical - 1 Sept 2008

Abarca Gabriela, Navarrete Marta, Trejos Rafael, de Céspedes Carlos, Saborío Manuel

Abstract excerpt

Hemoglobinopathies are hereditary autosomic recessive diseases. A total of 70 943 samples of whole blood collected by heel prick in filter paper (S&S 903) from throughout Costa Rica (October 2005-October 2006) were analyzed to detect variants of hemoglobin by the iso-electric focusing technique. Eight hundred ninety one cases presented some variant, for a frecuency of 1/79. Five cases are homozygous for...

Read the complete abstract on PubMed

Topics

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

Share to Anemia, Sickle Cell
Share to Costa Rica
Share to Genotype

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

Share to Incidence

Share to Infant, Newborn

Share to National Health Programs

Share to Neonatal Screening

Share to Phenotype

Source

Identifiers

PMID: 19419022

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

[Abnormal haemoglobins in the newborn human population of Costa Rica].PMID 19419022Read ↗

[Prevalence of abnormal hemoglobins in newborns in Natal, Rio Grande do Norte, Brazil].Semantic proximity Read ↗

Hemoglobinopathies in newborns in the southern region of the Triângulo Mineiro, Brazil. Cross-sectional study.Semantic proximity Read ↗

[Genetically based states of elevated quantity of foetal haemoglobin (Hb F) in healthy individuals and patients].Semantic proximity Read ↗

Reliability of isoelectrofocusing for the detection of Hb S, Hb C, and HB D in a pioneering population-based program of newborn screening in Brazil.Semantic proximity Read ↗

Prevalence of common hemoglobin variants in an afro-descendent Ecuadorian population.Semantic proximity Read ↗

Prevalence of sickle cell disease among Grenadian newborns.Semantic proximity Read ↗

Detection of the common Hb F Sardinia [A gamma (E19)Ile----Thr] variant by isoelectric focusing in normal newborns and in adults affected by elevated fetal hemoglobin syndromes.Semantic proximity Read ↗

Neonatal screening for haemoglobinopathies: the results of a 10‐year programme in an English Health RegionSemantic proximity Read ↗

[Hemoglobinopathy in Japan: detection and analysis].Semantic proximity Read ↗

Prevalence of sickle cell disease in a northeastern region of the Democratic Republic of Congo: what impact on transfusion policy?Semantic proximity Read ↗

The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island.Semantic proximity Read ↗

[Prevention of hemoglobinopathies in non-endemic countries].Semantic proximity Read ↗

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