Cytogenetic technology--genotype and 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

1. Comprehensive evaluation of the child with intellectual disability or global developmental delays.Pediatrics · 2014
   Pooled it
2. NGS-Based Diagnosis of Treatable Neurogenetic Disorders in Adults: Opportunities and Challenges.Genes · 2021
   Article
3. A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice.Journal of genetic counseling · 2014
   Article
4. Disease-targeted sequencing: a cornerstone in the clinic.Nature reviews. Genetics · 2013
   Article
5. Genetic counseling, activism and 'genotype-first' diagnosis of developmental disorders.Journal of genetic counseling · 2012
   Article
6. Review of genetic factors in intestinal malrotation.Pediatric surgery international · 2010
   Review
7. Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases.The Journal of molecular diagnostics : JMD · 2010
   Article
8. Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex.European journal of human genetics : EJHG · 2010
   Article
9. Multiple rare variants in the etiology of autism spectrum disorders.Dialogues in clinical neuroscience · 2009
   Review
10. Attention deficits, Attention-Deficit Hyperactivity Disorder, and intellectual disabilities.Developmental disabilities research reviews · 2008
    Review
11. Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature.European journal of medical genetics
    Review

Corrections and comments

• Comment on
  Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.2008

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as