ReviewAmerican journal of human genetics1996
How many breaks do we need to CATCH on 22q11?
Review in American journal of human genetics, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 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
10 citing papers in PubMed.
- Clinical Features of Aberrations Chromosome 22q: A Pilot Study.Global medical genetics · 2022Article
- A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review.BMC medical genetics · 2009Review
- HIRA, the human homologue of yeast Hir1p and Hir2p, is a novel cyclin-cdk2 substrate whose expression blocks S-phase progression.Molecular and cellular biology · 2001Article
- The DiGeorge anomaly.Clinical reviews in allergy & immunology · 2001Review
- 22q11 deletion syndrome: a genetic subtype of schizophrenia.Biological psychiatry · 1999Review
- Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion.American journal of human genetics · 1999Article
- Core histones and HIRIP3, a novel histone-binding protein, directly interact with WD repeat protein HIRA.Molecular and cellular biology · 1998Article
- 22q11 deletion syndrome in adults with schizophrenia.American journal of medical genetics · 1998Article
- Goosecoid-like sequences and the smallest region of deletion overlap in DiGeorge and velocardiofacial syndromes.American journal of human genetics · 1997Article
- Velocardiofacial syndrome.Postgraduate medical journal · 1997Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
8659546PMC1915098What 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.