Evidence map›Paper›PMID 35401667›Full record

ArticleFrontiers in genetics2022

Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in

Jianlong Zhuang, Chunnuan Chen, Yu'e Chen, Shuhong Zeng, Yuying Jiang, Yuanbai Wang, Xinying Chen, Yingjun Xie, Gaoxiong Wang

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 97% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 2 institutions in 1 country.

Jianlong ZhuangPrenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Chunnuan ChenDepartment of Neurology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Yu'e ChenUltrasonography, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Shuhong ZengPrenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Yuying JiangPrenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Yuanbai WangPrenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Xinying ChenPrenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Yingjun XieDepartment of Obstetrics and Gynecology, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Gaoxiong WangQuanzhou Women's and Children's Hospital, Quanzhou, China.
Fujian Medical University · CNThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

BCORchromosomal microarray analysisframeshift mutationhemizygous variantoculofaciocardiodentalwhole-exome sequencing

Identifiers

PMID35401667
PMCPMC8990034
OpenAlexW4221012390

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.