Evidence map›Paper›PMID 34012377›Full record

ArticleMolecular syndromology2021

Interstitial Deletion of 2q22.2q22.3 Involving the Entire

Khaled Refaat, Nivine Helmy, Mohamed Elawady, Mona El Ruby, Alaa Kamel, Mona Mekkawy, Engy Ashaat, Ola Eid, Amal Mohamed, Mervat Rady

Open access · bronzeAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular syndromology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Mowat-Wilson Syndrome: Case Report and Review ofInternational journal of molecular sciences · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Khaled RefaatDivision of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
Nivine HelmyDivision of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
Mohamed ElawadyDepartment of Community Medicine and Public Health, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Mona El RubyDepartment of Clinical Genetics, National Research Centre, Cairo, Egypt.
Alaa KamelDivision of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
Mona MekkawyDivision of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
Engy AshaatDepartment of Clinical Genetics, National Research Centre, Cairo, Egypt.
Ola EidDivision of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
Amal MohamedDivision of Human Genetics and Genome Research, Department of Human Cytogenetics, National Research Centre, Cairo, Egypt.
Mervat RadyDepartment of Community Medicine and Public Health, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
National Research Centre · EGAin Shams University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mowat-Wilson syndrome (MWS) is a rare autosomal dominant syndrome characterized by dysmorphic features, mental retardation, and congenital heart disease (CHD). MWS results from microdeletions of chromosome 2q23 or de novo SNVs involving the

Indexed as

Array CGHHirschsprung diseaseMowat-Wilson syndromeSyndromic congenital heart diseaseZEB2

Identifiers

PMID34012377
PMCPMC8114072
OpenAlexW3151492566

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.