ArticleAmerican journal of human genetics1997
Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region.
Article in American journal of human genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
What it found
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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
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Who cites it
15 citing papers in PubMed.
- The 22q11.2 Low Copy Repeats.Genes · 2022Review
- Cardiac Neural Crest.Cold Spring Harbor perspectives in biology · 2021Review
- Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.Human molecular genetics · 2019Article
- Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype.Journal of clinical laboratory analysis · 2019Article
- What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.American journal of medical genetics. Part A · 2018Article
- Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR.BMC medical genetics · 2014Article
- Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.PloS one · 2014Article
- The neural crest in cardiac congenital anomalies.Differentiation; research in biological diversity · 2012Review
- A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review.BMC medical genetics · 2009Review
- Detailed analysis of 22q11.2 with a high density MLPA probe set.Human mutation · 2008Article
- Constitutional growth delay pattern of growth in velo-cardio-facial syndrome: longitudinal follow up and final height of two cases.Journal of clinical research in pediatric endocrinology · 2008Article
- 22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.American journal of human genetics · 2008Article
- Genomic disorders on 22q11.American journal of human genetics · 2002Review
- Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.American journal of human genetics · 1999Article
- Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrum.European journal of medical geneticsArticle
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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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.