Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.

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, 30 citations in OpenAlex.

1. Molecular genetics of 22q11.2 deletion syndrome.American journal of medical genetics. Part A · 2018
   Review
2. Tuberous sclerosis, polycystic kidney disease and mucolipidosis III gamma caused by a microdeletion unmasking a recessive mutation.American journal of medical genetics. Part A · 2015
   Article
3. Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.PloS one · 2014
   Article
4. Discovery of variants unmasked by hemizygous deletions.European journal of human genetics : EJHG · 2012
   Article
5. Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size.Molecular cytogenetics · 2012
   Article
6. Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins.Journal of medical genetics · 2006
   Article
7. Genetic counselling for schizophrenia in the era of molecular genetics.Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2001
   Review
8. Genetic insights into schizophrenia.Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2001
   Review
9. 22q11 deletion syndrome: a genetic subtype of schizophrenia.Biological psychiatry · 1999
   Review
10. How many breaks do we need to CATCH on 22q11?American journal of human genetics · 1996
    Review

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.

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