Evidence map›Paper›PMID 33750428›Full record

ArticleMolecular cytogenetics2021

Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes.

Emanuele G Coci, Udo Koehler, Thomas Liehr, Armin Stelzner, Christian Fink, Hendrik Langen, Joachim Riedel

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular cytogenetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Emanuele G CociCenter of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany. Emanuele.Coci@akh-celle.de.
Udo KoehlerMedizinisch Genetisches Zentrum, 80335, Munich, Germany.
Thomas LiehrInstitute of Human Genetics, Friedrich Schiller University, Jena University Hospital, 07743, Jena, Germany.
Armin StelznerCenter of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany.
Christian FinkDepartment of Radiology, General Hospital of Celle, 29223, Celle, Germany.
Hendrik LangenCenter of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany.
Joachim RiedelCenter of Social Pediatrics and Pediatric Neurology, General Hospital of Celle, 29221, Celle, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID33750428
PMCPMC7941681

What OpenQuestion holds

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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.