Evidence map›Paper›PMID 1601428›Full record

ArticleHuman genetics1992

Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23.

L Warnich, I Groenewald, L Theart, A E Retief

Abstract read
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In one paragraph

Article in Human genetics, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

L WarnichDepartment of Human Genetics, Tygerberg Hospital, Republic of South Africa.
I Groenewald
L Theart
A E Retief

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The informativeness of locus D11S29 as a genetic marker was improved by the identification of a highly polymorphic (GT)n repeat within the locus. Ten alleles were identified in parents of 40 Centre d'Etude du Polymorphisme Humain families and the polymorphism information content (PIC) was 0.77. The increased PIC value thus enables refinement of the linkage map of 11q23.

Indexed as

Chromosomes, Human, Pair 11Repetitive Sequences, Nucleic AcidAllelesBase SequenceFemaleGene FrequencyGenetic LinkageGenetic MarkersHumansMaleMolecular Sequence DataPedigreePolymerase Chain ReactionPolymorphism, GeneticGenetic Markers

Identifiers

PMID1601428

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.