Evidence map›Paper›PMID 8557255›Full record

ArticleHuman genetics1996

Direct detection of disomy in human sperm by the PRINS technique.

F Pellestor, I Quennesson, L Coignet, A Girardet, B Andréo, J P Charlieu

Abstract read
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In one paragraph

Article in Human genetics, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Using PRINS for gene mapping in polytene chromosomes.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 1997
    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.

F PellestorCNRS UPR 9008, BP 5051, Montpellier, France.
I Quennesson
L Coignet
A Girardet
B Andréo
J P Charlieu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the use of the PRimedIN Situ (PRINS) labelling technique for the direct estimation of disomy rates for various chromosomes in human sperm. The PRINS technique provides a rapid and reliable method for chromosome screening since specific labelling may be obtained in less than 2 h. In the present study, the disomy rates of chromosomes 2, 5, 9, 12 and 18 were investigated. The incidences of disomy are similar for all these chromosomes, ranging from 0.27% to 0.33%. These findings suggest an equal distribution of aneuploidies among autosomes in human sperm.

Indexed as

AneuploidyBase SequenceChromosome MappingChromosomes, Human, Pair 12Chromosomes, Human, Pair 18Chromosomes, Human, Pair 2Chromosomes, Human, Pair 5Chromosomes, Human, Pair 9DNA PrimersHumansIn Situ Hybridization, FluorescenceMaleMolecular Sequence DataSpermatozoaDNA Primers

Identifiers

PMID8557255

What OpenQuestion holds

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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.