Evidence map›Paper›PMID 7913621›Full record

ArticleInternational journal of legal medicine1994

PCR typing of the locus D17S30 (YNZ22 VNTR) in an Italian population sample.

L Buscemi, N Cucurachi, R Mencarelli, B Sisti, A Tagliabracci, S D Ferrara

Abstract read
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In one paragraph

Article in International journal of legal medicine, 1994. 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.

L BuscemiIstituto di Medicina Legale dell'Università di Parma, Italy.
N Cucurachi
R Mencarelli
B Sisti
A Tagliabracci
S D Ferrara

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A sample of 202 subjects living in 2 Italian provinces (Ancona and Parma) was tested for YNZ22 polymorphism by the polymerase chain reaction (PCR). After amplification, the phenotypes were separated by agarose gel electrophoresis, stained with ethidium bromide and identified by comparison with a molecular weight marker. No heterogeneity was found between the 2 populations. Alleles, pooled in 4 groups to calculate the Hardy-Weinberg (H-W) equilibrium, showed good accordance between observed and expected values. The power of discrimination (PD) was 0.95 and the chance of exclusion was 0.69. The allele comparison with previous studies on Caucasians showed no significant difference.

Indexed as

Chromosome MappingGenetics, PopulationGenotypeAllelesDNAGene FrequencyGenetic Carrier ScreeningHumansItalyPaternityPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthRepetitive Sequences, Nucleic AcidDNA

Identifiers

PMID7913621

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.