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

[Assessment of the frequency of rare electrophoretic variants of blood proteins in children with congenital pathology].

TSitologiia i genetika - 1 Jan 2000

Afanas'ev K I, Suskov I I, Altukhov Iu P

Abstract excerpt

The frequency of rare electrophoretic protein variants was studied in children with congenital anomalies. The stated frequency (1.07 X 10(-3] proved to be ten-fold higher than in the control group of newborns (1.09 X 10(-4). This difference was mainly due to rare variants of monomorphic proteins. The data obtained confirm the assumption of a functional importance of monomorphic protein loci.

Read the complete abstract on PubMed

Topics

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

Share to Blood Protein Electrophoresis
Share to Blood Proteins
Share to Congenital Abnormalities

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

Share to Electrophoresis, Polyacrylamide Gel

Share to Genetic Variation

Share to Infant

Share to Infant, Newborn

Share to Phenotype

Source

Identifiers

PMID: 6729990

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

[Assessment of the frequency of rare electrophoretic variants of blood proteins in children with congenital pathology].PMID 6729990Read ↗

[Association between Kidd blood group and congenital malformations].Semantic proximity Read ↗

A polymorphic protein character of red blood cells (EP-1) in domesticated and wild sheep.Semantic proximity Read ↗

[Possibility of using the placental polymorphism of alkaline phosphatase in forensic serology].Semantic proximity Read ↗

[Human hemoglobin: polymorphism, neutrality of variants, evolutionary aspect].Semantic proximity Read ↗

[The significance of congenital inhibitor deficiency in acute pancreatitis].Semantic proximity Read ↗

[Genetic polymorphism of hemoglobin, protein systems, blood enzymes and their relationship to reproducibility].Semantic proximity Read ↗

[Frequency of phenotypes and genes of the polymorphic blood systems in a population as dependent on the age factor].Semantic proximity Read ↗

[Screening for alpha 1-antitrypsin deficiency in neonates].Semantic proximity Read ↗

[Genetic aspects of vitamin D-deficient rickets: genetic markers of blood].Semantic proximity Read ↗

Changes in the phenotype of polymorphic plasma proteins after liver transplantation - new data and medico-legal consequences.Semantic proximity Read ↗

[Rare phenotypes of alpha-1 antitrypsin: study of a case of the M1X variant].Semantic proximity Read ↗

[Prenatal diagnosis of mucoviscidosis: indication of enzyme determination and molecular biology techniques].Semantic proximity Read ↗

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