Evidence map›Paper›PMID 31871800›Full record

ArticleCase reports in genetics

Corrigendum to "Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features".

Jacquelyn D Riley, Catherine M Stefaniuk, Francine Erenberg, Angelika L Erwin, Lauren Palange, Caroline Astbury

Abstract readPublished Erratum
In one paragraph

Article in Case reports in genetics. 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

6 authors.

Jacquelyn D RileyMolecular Pathology Section, Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.ORCID https://orcid.org/0000-0001-9894-3282
Catherine M StefaniukMolecular Pathology Section, Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Francine ErenbergPediatric Cardiology, Pediatric Institute, Cleveland Clinic, Cleveland, OH, USA.
Angelika L ErwinCenter for Personalized Genetic Healthcare, Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Lauren PalangeCenter for Personalized Genetic Healthcare, Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Caroline AstburyMolecular Pathology Section, Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.ORCID https://orcid.org/0000-0001-6741-0010

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.1155/2019/5384295.].

Identifiers

PMID31871800
PMCPMC6906839

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.