Evidence map›Paper›PMID 39869287›Full record

ArticleGenes & genomics2025

Correction to: A novel frameshift TBX4 variant in a family with ischio-coxo-podo-patellar syndrome and variable severity.

Giada Moresco, Ornella Rondinone, Alessia Mauri, Rita Gorgoglione, Daniela Maria Grazia Graziani, Michal Dziuback, Monica Rosa Miozzo, Silvia Maria Sirchia, Luca Pietrogrande, Angela Peron and 1 more

Abstract readPublished Erratum
In one paragraph

Article in Genes & genomics, 2025. 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

11 authors.

Giada MorescoMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
Ornella RondinoneMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
Alessia MauriResearch Laboratories Coordination Unit, Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico, Milan, Italy.
Rita GorgoglioneMedical Genetics, ASST Santi Paolo e Carlo, Milan, Italy.
Daniela Maria Grazia GrazianiMedical Genetics, ASST Santi Paolo e Carlo, Milan, Italy.
Michal DziubackOrthopedics and Traumatology Unit, ASST Santi Paolo e Carlo, Milan, Italy.
Monica Rosa MiozzoMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
Silvia Maria SirchiaMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.
Luca PietrograndeOrthopedics and Traumatology Unit, ASST Santi Paolo e Carlo, Milan, Italy.
Angela PeronMedical Genetics, ASST Santi Paolo e Carlo, Milan, Italy. angela.peron@unifi.it.ORCID https://orcid.org/0000-0002-1769-6548
Laura FontanaMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID39869287
PMCPMC12638395

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.