ArticleJournal of medical genetics1996
Renal and urological tract malformations caused by a 22q11 deletion.
Article in Journal of medical genetics, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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
14 citing papers in PubMed.
- Anomalies of the genitourinary tract in children with 22q11.2 deletion syndrome.American journal of medical genetics. Part A · 2019Article
- Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.American journal of medical genetics. Part A · 2018Review
- 22q11 Deletion Syndrome and Urogenital Manifestations: A Clinicopathological Case Report.Frontiers in medicine · 2016Article
- 22q11.2 deletion syndrome.Nature reviews. Disease primers · 2015Review
- Practical guidelines for managing adults with 22q11.2 deletion syndrome.Genetics in medicine : official journal of the American College of Medical Genetics · 2015Review
- The role of ultrasound in the diagnosis of fetal genetic syndromes.Best practice & research. Clinical obstetrics & gynaecology · 2014Review
- Vesico-ureteric reflux: using mouse models to understand a common congenital urinary tract defect.Pediatric nephrology (Berlin, Germany) · 2011Article
- Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2.American journal of medical genetics. Part A · 2009Article
- Gene discovery and vesicoureteric reflux.Pediatric nephrology (Berlin, Germany) · 2008Review
- Microdeletion 22q11 and oesophageal atresia.Journal of medical genetics · 1999Article
- A population study of chromosome 22q11 deletions in infancy.Archives of disease in childhood · 1998Article
- Radial aplasia and chromosome 22q11 deletion.Journal of medical genetics · 1997Article
- Chromosome 22q11 deletion presenting as the Potter sequence.Journal of medical genetics · 1997Article
- How many breaks do we need to CATCH on 22q11?American journal of human genetics · 1996Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.