Evidence map›Paper›PMID 34304492›Full record

ArticleLin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery2021

[Genotype and phenotype analysis of a family with Waardenburg syndrome type Ⅰcaused by a novel mutation in

Xia Li, Shengbo Zhao, Xianyun Bi, Fan Lou, Wenjuan Zeng, Yan Gao, Zhiyong Mao, Jing Ma

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

Article in Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 91% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. A novel frameshift variant ofFrontiers in genetics · 2025
    Article
  2. [Analysis of molecular genetics and clinical characteristics of 3 children with Waardenburg syndrome].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2023
    Article
  3. [Evaluation of hearing and speech rehabilitation after cochlear implantation in children with Waardenburg syndrome].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2022
    Article
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

8 authors at 2 institutions in 1 country.

Xia LiDepartment of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
Shengbo ZhaoDepartment of Otolaryngology Head and Neck Surgery，Zhaotong First People's Hospital.
Xianyun BiDepartment of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
Fan LouDepartment of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
Wenjuan ZengDepartment of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
Yan GaoDepartment of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
Zhiyong MaoDepartment of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
Jing MaDepartment of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
Kunming Medical University · CNThe First People's Hospital of Zhaoqing · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Waardenburg SyndromeChinaGenotypeHumansMutationPAX3 Transcription FactorPedigreePhenotypePAX3 protein, humanPAX3 Transcription Factordeafness geneDNA mutational analysisgenotypePAX3Waardenburg syndrome

Identifiers

PMID34304492
PMCPMC10127909
OpenAlexW3186379445

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.