Use of array genomic hybridization technology for constitutional genetic diagnosis in Canada.

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

5 citing papers in PubMed.

1. Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.Human genetics · 2023
   Article
2. Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay.Scientific reports · 2016
   Article
3. Autism spectrum disorder: advances in evidence-based practice.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2014
   Review
4. Expanding probe repertoire and improving reproducibility in human genomic hybridization.Nucleic acids research · 2013
   Article
5. Risk factors for autism: translating genomic discoveries into diagnostics.Human genetics · 2011
   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

2 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.