Evidence map›Paper›PMID 1937466›Full record

ArticleHuman genetics1991

X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus.

L Van Maldergem, M Espeel, F Roels, C Petit, G Dacremont, R J Wanders, A Verloes, Y Gillerot

Abstract read
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In one paragraph

Article in Human genetics, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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

8 authors.

L Van MaldergemCentre de Génétique Humaine, Institut de Morphologie Pathologique, Loverval, Belgium.
M Espeel
F Roels
C Petit
G Dacremont
R J Wanders
A Verloes
Y Gillerot

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A case of X-linked recessive chondrodysplasia punctata (CP) is described. The finding of a reciprocal X-Y translocation involving the region distal to Xp22.3 and the presence of fluorescent Yp11.23 regions confirms the localization of X-linked recessive CP at p22.3. No gross peroxisomal abnormalities were present in the propositus.

Indexed as

Genes, RecessiveGenetic LinkageTranslocation, GeneticX ChromosomeY ChromosomeAdultChondrodysplasia PunctataDNAFemaleFetal DeathHumansImmunohistochemistryKaryotypingMaleMicrobodiesDNA

Identifiers

PMID1937466

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.