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

Two problematic human polymorphic Alu insertions.

Electrophoresis - 1 Jul 2003

Luis Javier R, Terreros Maria C, Martinez Laisel, Rojas Dina, Herrera Rene J

Abstract excerpt

Analysis of two previously described polymorphic Alu insertions (Sb19.3 and NBC3) in world-wide human populations generated genotypic frequencies grossly in violation of Hardy-Weinberg equilibrium expectations. GenBank searches at the National Center for Biotechnology Information (NCBI) and sequencing analyses revealed that samples homozygous for the Sb19.3 Alu insertion amplify a band indistinguishable in size...

Read the complete abstract on PubMed

Topics

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

Share to Alu Elements
Share to Diagnostic Errors
Share to DNA Primers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ethnicity

Share to Gene Frequency

Share to Genetic Markers

Share to Molecular Epidemiology

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 12874862
DOI: 10.1002/elps.200305451

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Two problematic human polymorphic Alu insertions.PMID 12874862Read ↗

Alu insertion polymorphisms for the study of human genomic diversity.Semantic proximity Read ↗

Genetic variation of recent Alu insertions in human populations.Semantic proximity Read ↗

Identification of a unique Alu-based polymorphism and its use in human population studies.Semantic proximity Read ↗

Identification and characterization of two polymorphic Ya5 Alu repeats.Semantic proximity Read ↗

High-resolution cartography of recently integrated human chromosome 19-specific Alu fossils.Semantic proximity Read ↗

The use of polymorphic Alu insertions in human DNA fingerprinting.Semantic proximity Read ↗

A dimorphic Alu Sb-like insertion in COL3A1 is ethnic-specific.Semantic proximity Read ↗

Long D13S317 variant allele: a cautionary case report.Semantic proximity Read ↗

A new three allele polymorphism at distal 21q22.3, a region relatively devoid of polymorphic markers. Mutations in brief no. 212. Online.Semantic proximity Read ↗

Polymorphisms within a polymorphism: SNPs in and around a polymorphic Alu insertion in intron 44 of the human dystrophin gene.Semantic proximity Read ↗

Allele non-amplification: a source of confusion in linkage studies employing microsatellite polymorphisms.Semantic proximity Read ↗

Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations.Semantic proximity Read ↗

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