The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease.

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.

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.

Who cites it

6 citing papers in PubMed.

1. An Anterior Second Heart Field Enhancer Regulates the Gene Regulatory Network of the Cardiac Outflow Tract.Circulation · 2023
   Article
2. Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing.Open life sciences · 2023
   Article
3. Transcription factor pathways and congenital heart disease.Current topics in developmental biology · 2012
   Review
4. Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.BMC medical genetics · 2011
   Article
5. Prenatal diagnosis of 22q11 deletions: a series of five cases with congenital heart defects.Journal of medical genetics · 1997
   Article
6. Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.Journal of medical genetics · 1997
   Article

Corrections and comments

• Comment on
  Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.1995

Authors and funding

6 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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