Evidence map›Paper›PMID 32184803›Full record

ArticleFrontiers in genetics2020

Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the

Lijing Shi, Hui Huang, Qiuxia Jiang, Rongsen Huang, Wanyu Fu, Liangwei Mao, Xiaoming Wei, Huanhuan Cui, Keke Lin, Licheng Cai and 3 more

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

Article in Frontiers in genetics, 2020. 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
0.6field-weighted citation impact, top 37% 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, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

13 authors at 3 institutions in 1 country.

Lijing ShiDepartment of Ultrasound, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Hui HuangBGI Genomics, BGI-Shenzhen, Shenzhen, China.
Qiuxia JiangDepartment of Ultrasound, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Rongsen HuangDepartment of Ultrasound, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Wanyu FuPrenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Liangwei MaoBGI-Wuhan Clinical Laboratories, BGI-Shenzhen, Wuhan, China.
Xiaoming WeiBGI-Wuhan Clinical Laboratories, BGI-Shenzhen, Wuhan, China.
Huanhuan CuiBGI Genomics, BGI-Shenzhen, Shenzhen, China.
Keke LinBGI Genomics, BGI-Shenzhen, Shenzhen, China.
Licheng CaiBGI-Guangzhou Medical Laboratory, BGI-Shenzhen, Guangzhou, China.
You YangBGI-Guangzhou Medical Laboratory, BGI-Shenzhen, Guangzhou, China.
Yuanbai WangPrenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, China.
Jing WuBGI Genomics, BGI-Shenzhen, Shenzhen, China.
BGI Group (China) · CNBGI GenomicsHubei University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Syndactyly is one of the most frequent hereditary limb malformations with clinical and genetical complexity. Autosomal dominant syndactyly type IV (SD4) is a rare form of syndactyly, caused by heterozygous mutations in a sonic hedgehog (

Indexed as

LMBR1sub-exome target sequencingsyndactyly type IVtibial and fibulal shorteningtriphalangeal thumb-polysyndactyly syndrome

Identifiers

PMID32184803
PMCPMC7058806
OpenAlexW3008473951

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.