Velocardiofacial syndrome and DiGeorge sequence.

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

11 citing papers in PubMed.

1. [DiGeorge syndrome/velcardiofacial syndrome: oral and maxillofacial surgery].HNO · 2003
   Trial
2. Multiple Intestinal Anomalies in a Newborn with 22q11.2 Microdeletion Syndrome: A Case Report and Literature Review.Journal of pediatric genetics · 2024
   Article
3. Lateral thinking in syndromic congenital cardiovascular disease.Disease models & mechanisms · 2023
   Article
4. Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.International journal of molecular sciences · 2017
   Review
5. Copy-number variation associated with congenital anomalies of the kidney and urinary tract.Pediatric nephrology (Berlin, Germany) · 2015
   Article
6. Global increases in both common and rare copy number load associated with autism.Human molecular genetics · 2013
   Article
7. Copy-number disorders are a common cause of congenital kidney malformations.American journal of human genetics · 2012
   Article
8. A copy number variation morbidity map of developmental delay.Nature genetics · 2011
   Article
9. Phenotypic variability and genetic susceptibility to genomic disorders.Human molecular genetics · 2010
   Review
10. Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
11. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.Human genetics · 1995
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as