Evidence map›Paper›PMID 27382416›Full record

ArticleMolecular cytogenetics2016

Erratum to: Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism.

Juliana Dourado Grzesiuk, Ciro Silveira Pereira, Carlos Henrique Paiva Grangeiro, Clarissa Gondim Picanço-Albuquerque, Flávia Gaona Oliveira-Gennaro, Filipe Brum Machado, Enrique Medina-Acosta, Ester Silveira Ramos, Maisa Yoshimoto, Lucia Martelli

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

Article in Molecular cytogenetics, 2016. 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

10 authors.

Juliana Dourado GrzesiukGenetics Department, Ribeirão Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14049-900 Brazil.
Ciro Silveira PereiraCenter of Biotecnology and Cellular Therapy, San Raphael Hospital, Salvador, 41253-190 Brazil.
Carlos Henrique Paiva GrangeiroGenetics Department, Ribeirão Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14049-900 Brazil.
Clarissa Gondim Picanço-AlbuquerqueGenetics Department, Ribeirão Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14049-900 Brazil.
Flávia Gaona Oliveira-GennaroGenetics Department, Ribeirão Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14049-900 Brazil.
Filipe Brum MachadoCenter of Biosciences and Biotechnology, Darcy Ribeiro State University of Northern of Rio de Janeiro, Campos dos Goytacazes, 28013-600 Brazil.
Enrique Medina-AcostaCenter of Biosciences and Biotechnology, Darcy Ribeiro State University of Northern of Rio de Janeiro, Campos dos Goytacazes, 28013-600 Brazil.
Ester Silveira RamosGenetics Department, Ribeirão Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14049-900 Brazil.
Maisa YoshimotoDepartment of Medical Genetics, Faculty of Medical and Dentistry, University of Alberta, Edmonton, Canada.
Lucia MartelliGenetics Department, Ribeirão Preto Medical School, University of Sao Paulo, Ribeirao Preto, 14049-900 Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.1186/s13039-016-0249-5.].

Identifiers

PMID27382416
PMCPMC4932718

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.