Evidence map›Paper›PMID 7599103›Full record

ArticleInternational journal of legal medicine1995

Suitability of the YNZ22 (D17S5) VNTR polymorphism for legal medicine investigations in the population of Catalonia (Spain).

M Gené, E Huguet, C Sánchez-García, P Moreno, J Corbella, J Mezquita

Abstract read
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In one paragraph

Article in International journal of legal medicine, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Polymorphism analysis of the VNTR locus D17S5 in central Spain.International journal of legal medicine · 1996
    Article
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

6 authors.

M GenéDepartment of Legal Medicine, Faculty of Medicine, University of Barcelona, Spain.
E Huguet
C Sánchez-García
P Moreno
J Corbella
J Mezquita

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allele and phenotype frequencies for the YNZ22 locus were determined in a population sample from Catalonia (Spain) using the polymerase chain reaction (PCR). In 311 unrelated individuals, 14 alleles and 56 phenotypes were observed. No deviation from Hardy-Weinberg equilibrium was found. The observed heterozygosity was 81.35%. The YNZ22 polymorphism is useful for paternity testing with a CE value of 70% and an Essen-Möller value of 9.35 (log.).

Indexed as

Chromosome MappingChromosomes, Human, Pair 17DNA ProbesPaternityPolymorphism, GeneticAdultAllelesChildFemaleGenetic MarkersHumansMaleMinisatellite RepeatsPhenotypePolymerase Chain ReactionSpainDNA ProbesGenetic Markers

Identifiers

PMID7599103

What OpenQuestion holds

Textmetadata
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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.